SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs13087 | snp | C/T | 0.483567 | 0.0891419 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82016855 | CCCATCTGCGGCCGA[C/T]GTGCTGGTGGCCAGG | 79058 |
rs2277707 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978925 | AGATGCCCGTGTTGC[G/T]GTACTGCAGGGGAAC | 79058 |
rs2277708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983465 | CGTGGATGGCGGGGC[A/G]TGGATGGTGGGACGG | 79058 |
rs4075239 | snp | C/G | 0.474544 | 0.10991 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000266 | CACTACTCTGGGCTG[C/G]GAGCCCCATGCTCCA | 79058 |
rs4461144 | snp | A/G | 0.192401 | 0.243274 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005321 | GGGGACCACTGCCCC[A/G]CAGGCCTCCGAGACC | 79058 |
rs4616350 | snp | C/T | 0 | 0 | intron-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009585 | TGCCTCAGTCGCCCC[C/T]ACATCCTGTCTGCAG | 79058 |
rs4796860 | snp | C/T | 0.00941946 | 0.067978 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81985599 | TGCTCACCTGATCTG[C/T]GGAAAATGGCTGAGA | 79058 |
rs4796863 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982258 | CAATGCGCTGGGCGC[A/G]GTGGCTCATGCCTGT | 79058 |
rs4969475 | snp | C/G | 0.498813 | 0.0243321 | utr-variant-3-prime | ASPSCR1 | GRCh38.p7 | 17:82017959 | CCTGCCCTGGTGCCC[C/G]AAGACAACTTTGAGG | 79058 |
rs4995642 | snp | A/G | 0.453209 | 0.145623 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013189 | CTCGGGGGCTGAGAG[A/G]GGACTGTCTCACCCC | 79058 |
rs6502045 | snp | C/T | 0.499965 | 0.00419314 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014548 | TCCCTGCCGAGGCAC[C/T]GTGGTGCCGCCTTCC | 79058 |
rs6502046 | snp | A/C | 0 | 0 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015652 | GCCTCTGGGCAGTGT[A/C]CCCTGGGCTTCTGTG | 79058 |
rs7207516 | snp | A/G | 0.485118 | 0.0849685 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987207 | GAGATGACGGAGCCT[A/G]AGAGCAAAGCGAAGC | 79058 |
rs7209747 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997104 | GGGATGAGGCCGTGT[C/G]CGCTCCGGGATGAGG | 79058 |
rs7209749 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997105 | GGATGAGGCCGTGTC[C/G]GCTCCGGGATGAGGC | 79058 |
rs7213474 | snp | C/T | 0.486855 | 0.0799975 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004842 | AGGCGGAAACCAGGC[C/T]GGGCTCAGCATGGCG | 79058 |
rs7213919 | snp | G/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997126 | GGGATGAGGCCGTGT[G/T]GGCTCCGGGATGAGG | 79058 |
rs7214612 | snp | A/G | 0.253264 | 0.249979 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997568 | tctcggctcactgca[A/G]cctctgccacccaag | 79058 |
rs7218409 | snp | A/G | 0.275732 | 0.248672 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006123 | CCAAGCACGCATGTG[A/G]ACCCGCAAGGACACA | 79058 |
rs7221618 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000656 | ATAAAGAGTCAGAAG[A/G]AAGAGACAGGATAAA | 79058 |
rs7222219 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997077 | tactgagacggTGGC[C/T]GTGTCTGCTCCGGGA | 79058 |
rs7222223 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997083 | gacggtggctgtgtC[C/T]GCTCCGGGATGAGGC | 79058 |
rs7222954 | snp | G/T | 0.18325 | 0.240924 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997488 | ttttttttttctggg[G/T]ttttttttttttttt | 79058 |
rs7223629 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995895 | GGCCAGAGAGGGCAC[A/G]TGGCCTGTGGTCCTG | 79058 |
rs7224889 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013558 | GGCAGGCAAGCAGGC[A/G]GCGGGCGCGGAAGCA | 79058 |
rs7405640 | snp | C/T | 0.483053 | 0.0904792 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991355 | GAGTGCATCTCAGCC[C/T]GTTCCTCCTTCTGTA | 79058 |
rs8074498 | snp | A/T | 0.499981 | 0.00306347 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996668 | GTGGGGGACAGAGAC[A/T]GGGGGGCCCTCCTGG | 79058 |
rs9890434 | snp | A/G | 0.153332 | 0.230554 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988665 | AGTGATTTGTGGCTG[A/G]CTGTTGTTGCTGGTG | 79058 |
rs9895794 | snp | A/C | 0.229429 | 0.249152 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006598 | AGGACGCCTCACCCC[A/C]GGTTGACGTCATTTT | 79058 |
rs9895872 | snp | C/T | 0.499694 | 0.0123573 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015025 | CTCAAAGGCCCTTCC[C/T]GGGCCCTGCTCTGGC | 79058 |
rs9896558 | snp | A/C | 0 | 0 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010547 | AAAAAAAAAAAAAAA[A/C]AAAAACCAGCACATT | 79058 |
rs9901214 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990752 | ACCCGgaggaggaaa[C/G]ggagtacctttctga | 79058 |
rs9904501 | snp | C/T | 0.197393 | 0.244402 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986377 | gcagttgcagtgagc[C/T]gagatcgcactgctg | 79058 |
rs9906594 | snp | C/G | 0.450487 | 0.149349 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977760 | ccgtccgccccgggc[C/G]ggcggccgcACCTGA | 79058 |
rs9906783 | snp | C/T | 0.24932 | 0.249999 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995747 | CTTGGGTCCCAGCTG[C/T]GGAGACCAGGCTGGG | 79058 |
rs9912335 | snp | C/T | 0.483563 | 0.0891524 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001783 | CCCGTCAGCCCTTCC[C/T]GGGCTCCCCCAGGAG | 79058 |
rs9912348 | snp | C/T | 0.49999 | 0.00219646 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001793 | CTTCCCGGGCTCCCC[C/T]AGGAGCAGCCTCCAG | 79058 |
rs9912517 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988497 | TGGGGCAGCTCTTTC[A/G]AGACACCAGGGACAG | 79058 |
rs9912553 | snp | C/G | 0.439085 | 0.163545 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001827 | CTGCCCTGCGGATGA[C/G]CCCCCTCACCAAACT | 79058 |
rs9916841 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984508 | cgtgaacccgggagg[C/G]ggagcttgcagtgag | 79058 |
rs11077964 | snp | G/T | 0.463666 | 0.129795 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008611 | GCAGGCGTGCATGGA[G/T]TCAGCCTGGCCATGG | 79058 |
rs11539915 | snp | G/T | 0 | 0 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81985534 | TTGCAGCTGGACGAT[G/T]GCTCGAGGTTGCAGG | 79058 |
rs11539916 | snp | C/T | 0.000345054 | 0.0131304 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81995996 | TCCTCCTGCAGGTGA[C/T]GGGTGAAGCTGCCCT | 79058 |
rs11539917 | snp | C/T | 0.0341531 | 0.126135 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81983635 | GCTGGAGATGGTGCC[C/T]GCTTCCCGGAGCCGT | 79058 |
rs11655288 | snp | G/T | 0.00470586 | 0.0482782 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986143 | GATGGCTGGGCACAG[G/T]GGCTGGGCACAGTGG | 79058 |
rs11658043 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986400 | cactgctgcactcca[A/G]cctgggcaacagaac | 79058 |
rs11869686 | snp | A/G | 0.0543475 | 0.155628 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004134 | AGGAGACCTCTGGGC[A/G]GTGTCCCGGCCTGTG | 79058 |
rs12150186 | snp | C/T | 0.102014 | 0.201495 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004255 | TGCTGTGAGGCCGCG[C/T]GCCCGCAGGGCTGCC | 79058 |
rs12150441 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002439 | tctgtgttctttgta[A/G]agaaggggttttgcc | 79058 |
rs12150442 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002441 | tgtgttctttgtaga[A/G]aaggggttttgccat | 79058 |
rs12937164 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984950 | acccgcacacacCCG[C/G]ACACACCCcacacac | 79058 |
rs12937344 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986233 | gttcaagactagcct[C/T]ggcaacatagtgaaa | 79058 |
rs12938990 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009666 | AGGCACAGCTCTGAG[C/G]GGGCCCCCTGTGAGG | 79058 |
rs12939600 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009828 | TGGGGGCGACTGAGG[C/T]ACAGCTCTGAGCAGG | 79058 |
rs12944078 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009675 | TCTGAGCGGGCCCCC[C/T]GTGAGGTCTGTGGAC | 79058 |
rs12944349 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009748 | TGTGAGGTCTGTGGA[C/T]GGGACGTGGGGGCGA | 79058 |
rs12944359 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009770 | TGGGGGCGACTGAGG[C/T]ACAGCTCTGAGGGGG | 79058 |
rs12946118 | snp | C/G | 0.434232 | 0.168992 | intron-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009610 | GAGGCACAGCTCTGA[C/G]GGGGCCCCCCGTGAG | 79058 |
rs12946643 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009749 | GTGAGGTCTGTGGAT[A/G]GGACGTGGGGGCGAC | 79058 |
rs12946652 | snp | G/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009758 | GTGGATGGGACGTGG[G/T]GGCGACTGAGGTACA | 79058 |
rs12946671 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009782 | AGGTACAGCTCTGAG[C/G]GGGCCCCCTGTGAGG | 79058 |
rs12952898 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009691 | GTGAGGTCTGTGGAC[A/G]GGACGTGGTGGCGAC | 79058 |
rs34085048 | snp | A/G | 0.0420396 | 0.138753 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82009055 | GTGGACCGGGAGCCC[A/G]TGGACCGGGAGCCGG | 79058 |
rs34231047 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81998949 | TGACCCTCTCCCTCA[C/T]GCCTCCCCCCAACCG | 79058 |
rs34248146 | in-del | -/A | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006262 | GCATGCTTGGGGGGC[-/A]GTGTGCGTGTCCTTG | 79058 |
rs34276642 | in-del | -/CG | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009695 | GGTCTGTGGACAGGA[-/CG]TGGTGGCGACTGAGG | 79058 |
rs34286048 | in-del | -/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81998623 | GGTGTTGAACCGTTT[-/T]CAGTGTTTTCAGCAT | 79058 |
rs34397124 | in-del | -/A | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005564 | CCACACACCTGGGGG[-/A]CCCCACCAAGGCTGA | 79058 |
rs34430138 | in-del | -/A | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994943 | TTCCAACTGGAAAAT[-/A]CTGCTGTCCCGCAGC | 79058 |
rs34477876 | in-del | -/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010170 | CAGGTGATCTGCCCG[-/C]CTCGGCCTCCCAAAG | 79058 |
rs34493879 | in-del | -/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002084 | CAATTACGGCTCACA[-/G]GCAGTCATGACCTTC | 79058 |
rs34501574 | in-del | -/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984370 | TCACCTGAGGTCAGG[-/T]AGTTTGGGACCAGCC | 79058 |
rs34550798 | in-del | -/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005660 | CTTGGGAGCTTTCCA[-/G]GTGGGGATGTTTGTA | 79058 |
rs34569308 | in-del | -/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006211 | CCTTGCATGTGCACA[-/G]GTGTGTGTGTGTGTG | 79058 |
rs34713087 | snp | C/G | 0.029116 | 0.117091 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005549 | AGGGACACCTGGCGG[C/G]CACACACCTGGGGGA | 79058 |
rs34809841 | in-del | -/C | | | upstream-variant-2KB, intron-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977064 | GGACCGTCGCGGCAG[-/C]CCTAGGGCTGCCAGA | 79058 |
rs34821926 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983888 | TTTGAGCTGGAGTCT[C/T]GCTCTGTCGCCCAGG | 79058 |
rs34996654 | in-del | -/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009700 | GTGGACAGGACGTGG[-/T]GGCGACTGAGGCACA | 79058 |
rs35006864 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983513 | TGGCAGGGCGTGTCA[A/G]GCTCTGCAGGGCAGC | 79058 |
rs35134723 | in-del | -/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994325 | GCCCCTCCCTCCATG[-/C]TTCGGTGACATCAGG | 79058 |
rs35211881 | in-del | -/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988951 | GCGGCTCTCACCTGT[-/G]AATCCCAGCACTTTG | 79058 |
rs35252476 | in-del | -/C | | | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978030 | GTACTCGGCGCCCGG[-/C]CGAGCCCAGCTCGCG | 79058 |
rs35308604 | in-del | -/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005298 | CATCAGTTGGGCCCT[-/G]GGGGTTTGGTCTCGG | 79058 |
rs35344256 | snp | A/C | 0.430732 | 0.172731 | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976318 | TCTTCAAAAACGCCA[A/C]TAAAGAATTAAAACC | 79058 |
rs35432990 | in-del | -/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988527 | CAGGAGGTGGTGGGG[-/C]CCGTTGGTGGTAAAG | 79058 |
rs35470321 | in-del | -/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989396 | AGGTCTGCATGAGGG[-/C]AGGGAGGCTCTCGTG | 79058 |
rs35536513 | in-del | -/A | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985306 | ATGCACACACGCATG[-/A]CTGGTGCAGCCCTGC | 79058 |
rs35800056 | in-del | -/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995310 | ACTGGCCCGGAGGGG[-/C]CCTGGGGGGCCAGGA | 79058 |
rs35834288 | snp | A/G | 0.493107 | 0.0583 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978065 | CGCCGGGAAGAGGGA[A/G]GAGTGGAGCCCTAGA | 79058 |
rs35882908 | snp | G/T | | | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81975780 | TTTTTTTTTTTTTTT[G/T]TGAGACAGAGTCTTG | 79058 |
rs35890420 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81994849 | ACCCCGGCGGGGCCA[-/C]CCCCAGTCTGCGTGT | 79058 |
rs35893455 | in-del | -/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997895 | TGGTGGCGCACTTTC[-/G]GGCTCACTGTAACCT | 79058 |
rs35940283 | in-del | -/A | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008807 | GGTGCACTGACTGGG[-/A]AGAGGGGGGTCTCCA | 79058 |
rs35945308 | snp | G/T | 0 | 0 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004764 | CTCTGACTCTGCCCA[G/T]CAAGAGGGGCAGGGT | 79058 |
rs35972820 | in-del | -/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988934 | TTTCCAGGCCGGGCA[-/T]TGGCGGCTCTCACCT | 79058 |
rs36093868 | in-del | -/T/TT | 0.5 | 0 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009915 | ATTTAGAATGAAACC[-/T/TT]TTTTTTTTTTTTTGA | 79058 |
rs41283357 | snp | C/G | 0.304688 | 0.243945 | upstream-variant-2KB, intron-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977026 | TGAAACCGGTCTCCC[C/G]CCTTTCCTACCCTCA | 79058 |
rs41283359 | snp | G/T | 0 | 0 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997148 | GGGATGAGGCCGTGT[G/T]GGCTCCATGACAAGG | 79058 |
rs55671960 | snp | C/T | 0.18134 | 0.240387 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81979110 | GGAAGCTGAATGCCC[C/T]TGGCTGACCTGGCCC | 79058 |
rs55690610 | in-del | -/GT | 0.490635 | 0.0677858 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006212 | CTTGCATGTGCACAG[-/GT]GTGTGTGTGTGTGTG | 79058 |
rs55733420 | in-del | -/A | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984593 | TCAAAAAAAAAAAAA[-/A]GAGCAGCAAACATTT | 79058 |
rs55782107 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997431 | CCACCTCCTACCTGA[A/G]CAGGGTCACTGGGCT | 79058 |
rs56325683 | snp | A/C | 0.200801 | 0.245111 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985393 | GGGGTCAGCCTCTCC[A/C]TGGAGGCCAGGGCGG | 79058 |
rs57221908 | snp | C/T | 0.102014 | 0.201495 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993338 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACCA | 79058 |
rs57407294 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985263 | ATATGCACACACGCA[C/T]GCACACCTGCACATA | 79058 |
rs57441973 | snp | C/T | 0.0923359 | 0.194016 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013458 | AGCCTCGGGGCCTCT[C/T]GGGGTGGTGTCCCCG | 79058 |
rs58162523 | in-del | -/CCACGCACAC | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985058 | CCCCCCCACACACAC[-/CCACGCACAC]ACCTGTACACACACA | 79058 |
rs58325247 | snp | A/G | 0.135825 | 0.222405 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81998950 | GACCCTCTCCCTCAC[A/G]CCTCCCCCCAACCGT | 79058 |
rs58866411 | snp | C/T | 0.495056 | 0.049474 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010515 | GCCTGGGCGACAGAG[C/T]GAGACTCCATCTCAA | 79058 |
rs59513476 | snp | C/T | 0.106278 | 0.204558 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005136 | GGCTTTGGGGAGCAG[C/T]GGGAGGCCTGGGGGT | 79058 |
rs59606152 | snp | C/T | 0.255127 | 0.249947 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995068 | CCCCGAAACCTCCCT[C/T]GGCGCCCTGTTTGTT | 79058 |
rs59613601 | snp | A/C | 0.24932 | 0.249999 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995396 | GGTTCAGGTCTACGT[A/C]CTCCCTTGAGGGGAT | 79058 |
rs60146039 | snp | C/G | 0.143284 | 0.226079 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993404 | ATTTTTAGTAGAGAC[C/G]GGGTTTCATTGTGTT | 79058 |
rs60183079 | snp | A/C | 0.0189856 | 0.0955633 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012599 | CGGCAGCAGTCCCTG[A/C]CCAGGGGTCTGGGTG | 79058 |
rs60265923 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005248 | TGGCAGGGTGGGGCG[C/T]CGGGGTGGCGGAAAC | 79058 |
rs60293637 | snp | C/T | 0.135825 | 0.222405 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000691 | AGGCAGGTCCTCGGC[C/T]GAGACCCGGGGTGGT | 79058 |
rs60295754 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000441 | CGTCCTGCCTGCCCC[A/G]CGCCTCCCATCGCCG | 79058 |
rs60666195 | snp | C/G | 0.0256215 | 0.110247 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995219 | CGTGGCGGGACCCTC[C/G]TAGCGCTCGTCCCTG | 79058 |
rs61124385 | snp | G/T | 0.152334 | 0.230133 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991703 | GTCTAGCCGCTTGGC[G/T]GCTGGGCTGTCATGT | 79058 |
rs61457271 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999237 | TGCCAGCTGCCAGCC[A/C]CAGCCCAGGGGCCAG | 79058 |
rs61533596 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993292 | GATCTCGGCTCACTG[C/T]AAGCTCCACCTCCTG | 79058 |
rs61738267 | snp | C/G | 0.090703 | 0.192677 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996536 | AATCTGGGGAGCTCA[C/G]CCGCGGCGACTTGAG | 79058 |
rs62078703 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983024 | TATTTTTGTATTTTC[A/G]GTAGAGACGGGGTTT | 79058 |
rs62078704 | snp | C/T | 0.5 | 0 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008693 | GCTCTAATTTGGCGG[C/T]TGTCGCCACCCCTCC | 79058 |
rs62078705 | snp | A/G | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant, missense | ASPSCR1 | GRCh38.p7 | 17:82017394 | CAGGAATAAAGACTT[A/G]TGCATCCCTCAACGC | 79058 |
rs71166182 | in-del | -/GGGCTCCGGGATGAGGCCGTGT | 0 | 0 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997147 | GGGATGAGGCCGTGT[-/GGGCTCCGGGATGAGGCCGTGT]TGGCTCCATGACAAG | 79058 |
rs71166183 | in-del | -/T | 0 | 0 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002004 | TTTTTTTTTTTTTTT[-/T]GAGACACAGTCTCGC | 79058 |
rs71367094 | in-del | -/G | 0.5 | 0 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005814 | GGATGTGGGAAGGGG[-/G]CGGAGGCACAGCTCC | 79058 |
rs71375066 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013740 | GTGCAGGTTTTCTGG[A/G/T]AGGGCTGGGAGGAGG | 79058 |
rs71375067 | snp | C/G | 0.5 | 0 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013755 | GAGGGCTGGGAGGAG[C/G]CGGCCAGGAGTGAGG | 79058 |
rs72038922 | in-del | -/CACACCCACG | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985053 | CACCTCCCCCCCACA[-/CACACCCACG]CACACACCTGTACAC | 79058 |
rs72861716 | snp | A/C | 0.097727 | 0.198275 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001903 | GACACACGCCTGCCA[A/C]ACCGTAACGTGCCCA | 79058 |
rs72861721 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010982 | CTGCGGGCTCCAGGG[C/G]ACTGGGTGGGTGCGG | 79058 |
rs73356117 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985949 | TCCCCATGCTTGATT[A/C]CCCTGGATGGGATCA | 79058 |
rs73356119 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997230 | GGCCGCCCTGGGGTG[C/G]TGCATGGAGGGCAGC | 79058 |
rs74002712 | snp | A/G | 0.166832 | 0.235761 | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976663 | GGGCAGCTGAGCCCT[A/G]GCCAGGAGTCCGCAG | 79058 |
rs74002713 | snp | C/G | 0.176219 | 0.238865 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81979665 | GACCCATCTTTTTTG[C/G]GGGGGCCACCATTCA | 79058 |
rs74002714 | snp | A/G | 0.153332 | 0.230554 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982498 | AGCCTGCCTGCCCTC[A/G]GGATCCCCCGATCTG | 79058 |
rs74002715 | snp | C/T | 0.158632 | 0.232706 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987217 | AGCCTGAGAGCAAAG[C/T]GAAGCCACGGGCAGG | 79058 |
rs74002716 | snp | A/G | 0.135825 | 0.222405 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001176 | GGCTGGGCCTGGAGC[A/G]GGTCATGCACTGGGC | 79058 |
rs74002718 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004478 | AAAGGGGCAGAAGCA[C/T]GCAGGGGCTTCACCT | 79058 |
rs74002719 | snp | G/T | 0.0232847 | 0.105357 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005289 | GTGAAGTGGGCATCA[G/T]TTGGGCCCTGGGGTT | 79058 |
rs74004975 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008085 | CCCACAGCAGTCGAG[A/G]TCTCAGGTGTGTCCG | 79058 |
rs74004976 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016738 | GCTGGTGGGCAGATG[C/T]TGGGTGGATGGTGAG | 79058 |
rs74327286 | snp | A/C | 0.5 | 0 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988150 | CGAGACTCTGTCTCA[A/C]AAAAAAAAAAAAAAG | 79058 |
rs74402017 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993721 | CCTCCCAGTACCCCC[C/T]ATCCCGGAGGGTTGC | 79058 |
rs74544558 | snp | A/C | 0.5 | 0 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988151 | GAGACTCTGTCTCAA[A/C]AAAAAAAAAAAAAGA | 79058 |
rs74629517 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006264 | CATGCTTGGGGGGCG[C/T]GTGCGTGTCCTTGCG | 79058 |
rs74671544 | snp | A/C | 0 | 0 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988457 | AGGACTCCGTCTCAA[A/C]AAAAAAAAAAAAAAC | 79058 |
rs74795907 | snp | A/G | 0.0125593 | 0.0782427 | synonymous-codon, nc-transcript-variant, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82017097 | GGGCAAGGTGCCCAA[A/G]TGGCTGAAGCTGCCG | 79058 |
rs74883953 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988644 | ACACTCACACCTGTG[A/G]TGGAGAGTGATTTGT | 79058 |
rs75232864 | snp | A/T | | | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81975789 | TTTTTTTTGAGACAG[A/T]GTCTTGCTCCGTCTC | 79058 |
rs75338132 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000981 | GCCCGCACGGGCTGG[C/T]GGCTGCTGCCCTGCC | 79058 |
rs75356884 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015447 | GCCTACTTCCCTCTC[C/T]TGGTGTTCCCGAGTC | 79058 |
rs75454886 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989748 | CCTGGCCCGACCAGC[A/G]TCTCAAGCAGCAGGG | 79058 |
rs75578065 | snp | A/G | 0.5 | 0 | intron-variant, utr-variant-5-prime | ASPSCR1 | GRCh38.p7 | 17:81981243 | ATCCCTTAGGGAAGA[A/G]AGCCTGCAGATGTGT | 79058 |
rs75607123 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994599 | CGCACCACAGGCCAG[A/G]GTCCTTGGGAGCGCC | 79058 |
rs75669493 | snp | A/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016147 | CCGCCAGGACCCGCC[A/T]CGCCTGGCCCCACCT | 79058 |
rs75703546 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988747 | GCCATGCTCTTCCGT[C/T]GTGTGGGTGTCATGT | 79058 |
rs75711152 | snp | A/G | 0.0670745 | 0.170406 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014444 | CCCTGCCCAGGCACC[A/G]TGGTGCCTTCTCTCT | 79058 |
rs76001977 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003735 | ATGCCTGTCCACGCC[A/G]GTCGCAGCGGTCTCC | 79058 |
rs76218591 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005269 | TGGCGGAAACATGAG[A/G]CCGCGTGAAGTGGGC | 79058 |
rs76496634 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987622 | CTGGAGAGGTGGGGC[C/T]GGCATTGTGGTAGCA | 79058 |
rs76591849 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987514 | GGTGAGGGCCGTCCT[C/T]CCTGGCTGTGCTGTC | 79058 |
rs76819814 | snp | A/G | 0.0685596 | 0.171987 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008456 | CACTGTGCTGAATGC[A/G]TTGAAATCACTGCCC | 79058 |
rs76963416 | snp | G/T | 0.148661 | 0.22854 | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81975860 | GCTCTGCCTCCCGGA[G/T]TCACGCCATTCTCCT | 79058 |
rs77036984 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001570 | CAGGCGCTTGTGTTT[C/T]GGTGAGGAACCCCGG | 79058 |
rs77153203 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016150 | CCAGGACCCGCCACG[C/T]CTGGCCCCACCTTCC | 79058 |
rs77309715 | snp | A/T | 0.5 | 0 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993843 | CCTTGCAAGGCACAC[A/T]GGCCATAGGGCCTGG | 79058 |
rs77427192 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991941 | GAGCGGGGCCCCAGC[A/G]GGGCGGGGTTTGTGG | 79058 |
rs77437037 | in-del | -/TCCCGGCAGCTG | 0.00279162 | 0.0372561 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000920 | CCCCACAACTCGGCC[-/TCCCGGCAGCTG]GCACGAGGGCCGCTC | 79058 |
rs77493122 | snp | C/T | 0.00565429 | 0.0528694 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016794 | TGAGCTTGGGCCTCC[C/T]TGCAGGTGTCTACCT | 79058 |
rs77778838 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016149 | GCCAGGACCCGCCAC[C/G]CCTGGCCCCACCTTC | 79058 |
rs78060529 | snp | C/G | 0.274124 | 0.248833 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81980260 | TACTGGGATTACAGA[C/G]ATGAGTCACCATGCC | 79058 |
rs78103928 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995880 | GGTGGGTAGGATGGA[A/G]GCCAGAGAGGGCACG | 79058 |
rs78274313 | snp | A/G | 0.0838263 | 0.186779 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008991 | GCCCGGGGTGCGGAG[A/G]GCCCAGCCCGTGACA | 79058 |
rs78593363 | snp | C/G | 0.0460142 | 0.144533 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003574 | TGGGGGCGGCGCCGT[C/G]TCCTCTGGGTGGGAT | 79058 |
rs78770808 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001947 | TCATGGTCAGCCCAG[A/G]CTGCAGCAGTCCTGA | 79058 |
rs78996684 | snp | C/G | 0.5 | 0 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984238 | TGTCAGCAGCATTCA[C/G]CCACCAGCCTGACCA | 79058 |
rs79060512 | snp | A/G | 0.0919752 | 0.193722 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001301 | CTGGACCCTGACGCC[A/G]GGCTAGACAGGAGCC | 79058 |
rs79086817 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993003 | CAGGCTGTCAGAGTC[A/G]GGGCCTGGGTGGGAA | 79058 |
rs79173732 | snp | C/T | 0.0718919 | 0.175435 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006747 | TTTTTTCCCTCACAG[C/T]GTCTCATCCCTCAAC | 79058 |
rs79353595 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007367 | ATTTTTTCAGTTTTG[C/T]TTTCCAAATGAAGTC | 79058 |
rs79461463 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989258 | ACCCAAGCTTTGTCC[C/T]AGAAGCTGGAGTTTG | 79058 |
rs79469172 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999033 | CCCTGTCCTGACCCC[G/T]CATCAGAGCCCTGCA | 79058 |
rs79496236 | snp | C/T | 6.59e-05 | 0.00573983 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81979219 | GCGGCAGGACTTCAA[C/T]CCCTGTGAATATGAT | 79058 |
rs79705591 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014999 | GGAGAGGCCCCTCAG[C/T]CTGTGCCTCCCTCAA | 79058 |
rs79781074 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992365 | CCTCCCTGAGATCCC[A/G]CATGAGGGAGGGAAT | 79058 |
rs79976887 | snp | G/T | 0.0197687 | 0.0974348 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990989 | GTGGTGAAAGGCAGG[G/T]GTGTGGATGGACCAT | 79058 |
rs80039090 | snp | G/T | 0.0539704 | 0.155153 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011737 | TGGCCTCCCGCCCAG[G/T]TGCCTCCTGCAGCCC | 79058 |
rs80130302 | snp | G/T | 0.0566069 | 0.158427 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992629 | CCTGGGCCCTCCCTG[G/T]CCCCCTTCCTGGCCC | 79058 |
rs80249348 | snp | A/C | 0 | 0 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999628 | TGAAACTCCATCTCA[A/C]AAAAAAAAAAAAAAA | 79058 |
rs80286701 | snp | G/T | 0.089084 | 0.191327 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983851 | CTGGCAACTGAAAAT[G/T]AGCATCTCATGTTTT | 79058 |
rs80320521 | snp | A/G | 0.0456336 | 0.143994 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003566 | GCTCAGCCTGGGGGC[A/G]GCGCCGTCTCCTCTG | 79058 |
rs80342937 | snp | G/T | 0.5 | 0 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981346 | CTGGTTCAGTTGGTT[G/T]GGGGGGGCTTAGGGT | 79058 |
rs111271806 | snp | A/C | 0.0551013 | 0.156571 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994434 | GACGTCGGTACCCTG[A/C]CTCTCAGGCTCCTGA | 79058 |
rs111277254 | snp | C/T | 0.0107607 | 0.0725574 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82010834 | GTTCCCCGACCGCTA[C/T]GTCCTACAGGGCTTC | 79058 |
rs111319132 | snp | A/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983306 | AAGGAGCAGCCCCCT[A/C]GGCGTGCACCGAGGC | 79058 |
rs111348786 | snp | A/G | 0 | 0 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006263 | GCATGCTTGGGGGGC[A/G]TGTGCGTGTCCTTGC | 79058 |
rs111357111 | snp | C/T | 0.5 | 0 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999207 | CCCAGCCCCTGTGTC[C/T]CCTGAGGGCCAGGCT | 79058 |
rs111505488 | snp | A/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984839 | CACACCCCCACACAC[A/C]CCTGCACACACCCCA | 79058 |
rs111633399 | snp | C/T | 6.90441e-05 | 0.00587514 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996557 | GCGACTTGAGCCGTC[C/T]GGAGGACGCGGACAC | 79058 |
rs111649076 | snp | G/T | 0.5 | 0 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008297 | GCCAAGCCATCCCCA[G/T]GTGTCGAGAGTGTGA | 79058 |
rs111656919 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978646 | GGTCCCCAGGCCTGG[A/G]CAGGTGGAGGGCGCA | 79058 |
rs111699244 | in-del | -/G | 0.464629 | 0.128197 | intron-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009621 | CTGAGGGGGCCCCCC[-/G]TGAGGTCTGTGGACG | 79058 |
rs111790261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008479 | CACTGCCCAGGGCTC[C/T]GCGAGCTGCACGGCC | 79058 |
rs111889117 | snp | C/T | 0.5 | 0 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987093 | AGCCTAAGAGCAAAG[C/T]GAAGCCACGGGCAGG | 79058 |
rs111891945 | snp | C/T | 1.70766e-05 | 0.00292199 | utr-variant-3-prime, nc-transcript-variant, missense | ASPSCR1 | GRCh38.p7 | 17:82017370 | CCACAGGACCACCTC[C/T]TCTGCCAGCAGGAAT | 79058 |
rs111955317 | snp | G/T | 0.5 | 0 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010333 | AGGAGATCGAGACCA[G/T]CCTGGCTGACACGGT | 79058 |
rs111978156 | snp | C/G | 0.0341408 | 0.126114 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990351 | GAGGGCGTCAGGAGA[C/G]AGAGGCTGCACACTG | 79058 |
rs112054193 | snp | A/T | 0.5 | 0 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82016516 | TGCACTTGGGAGCCG[A/T]GGAGCCGGCAGGTGA | 79058 |
rs112055269 | snp | A/G | 0.163236 | 0.234461 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978102 | TTCCCATTCCGGGGC[A/G]TCCCCCGGAGCGGGA | 79058 |
rs112056046 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995418 | TGAGGGGATGAGCCA[C/T]GGGGCTCAGGACCCA | 79058 |
rs112236115 | in-del | -/G | 0 | 0 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995970 | TGCAAGGCGCACCTG[-/G]TCCTGGCTGCTCCTC | 79058 |
rs112273062 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012604 | GCAGTCCCTGCCCAG[A/G]GGTCTGGGTGAGGAA | 79058 |
rs112301403 | snp | A/C | 0.5 | 0 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008163 | CACCCTGGCTGTCAC[A/C]CAGTGTGGGCATGGT | 79058 |
rs112325498 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013416 | CCCTACCAGCCACCG[C/T]CTCCTGCCCTCCATC | 79058 |
rs112334232 | in-del | -/CCGT | 0 | 0 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005860 | GTGTGTGTGGGAAAA[-/CCGT]CCGGGTACTTGGGGA | 79058 |
rs112338243 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989518 | TTCTTTCATGTGTTT[C/T]GGAGGAGGTCTGAGT | 79058 |
rs112403819 | snp | C/G | 0.00465645 | 0.0480265 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82016804 | CCTCCCTGCAGGTGT[C/G]TACCTGGAGCCTGGC | 79058 |
rs112483517 | snp | C/T | 0.5 | 0 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005838 | CAGCTCCAGCCCCAG[C/T]GTGACCGTGTGTGTG | 79058 |
rs112485624 | snp | A/G | 0 | 0 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001895 | TCCACAGTGACACAC[A/G]CCTGCCACACCGTAA | 79058 |
rs112704842 | snp | A/C | | | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978525 | AGCGAGACTCCATAT[A/C]AAAAAAAAAAAAAAA | 79058 |
rs112737799 | snp | C/T | 0.245916 | 0.249967 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987816 | CGCACCATTGCACTC[C/T]AGCCTGGGTGACAAG | 79058 |
rs112762055 | snp | C/T | 0 | 0 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005337 | GGGGCAGTGGTCCCC[C/T]GGCTCTTGCTGCCCT | 79058 |
rs112771220 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011234 | CTGTACCCAGACGGC[C/T]GGGCGGCAGCAGCCC | 79058 |
rs112871069 | snp | C/T | 0.111224 | 0.207945 | downstream-variant-500B, intron-variant, utr-variant-3-prime | ASPSCR1 | GRCh38.p7 | 17:82017670 | CCAGGAGCCAAGCCC[C/T]GGGCCAGGAGCTGGG | 79058 |
rs112936918 | snp | A/G | 0.00286874 | 0.0377643 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994954 | AAAATCTGCTGTCCC[A/G]CAGCCGTCTCCAGGG | 79058 |
rs112938817 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014702 | GAGGGGGCGGCCAGG[C/T]GCTGGGCCACGTGTG | 79058 |
rs113129849 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982422 | ACTTGCTTACAAAGT[A/G]CAGCCGGTGCAGAGG | 79058 |
rs113247132 | snp | C/T | 0 | 0 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995065 | CTGCCCCGAAACCTC[C/T]CTCGGCGCCCTGTTT | 79058 |
rs113259462 | snp | C/T | 0 | 0 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014450 | CCAGGCACCGTGGTG[C/T]CTTCTCTCTCCCGGG | 79058 |
rs113339393 | in-del | -/G | 0 | 0 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995974 | AGGCGCACCTGTCCT[-/G]GGCTGCTCCTCCTGC | 79058 |
rs113343287 | snp | A/G | 0 | 0 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984949 | CACCCGCACACACCC[A/G]CACACACCCCACACA | 79058 |
rs113441884 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006869 | CTCACCAGTCAACAG[A/G]GCTGGGTGTGGCTGG | 79058 |
rs113494219 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004414 | CTCCTGGAGGCCGGG[A/G]CCTGGGGGTCCACCG | 79058 |
rs113495237 | snp | C/T | 0 | 0 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001506 | AGATGGCTCAGCGAC[C/T]TTGCAGGTGGCTGGC | 79058 |
rs113732613 | snp | A/G | 0.5 | 0 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995288 | CCCTTTGCTGGGGTG[A/G]GGGGGCACTGGCCCG | 79058 |
rs113733444 | snp | A/G | 0 | 0 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009667 | GGCACAGCTCTGAGC[A/G]GGCCCCCTGTGAGGT | 79058 |
rs113734324 | snp | A/G | 0.5 | 0 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991424 | CAGCCCTCTGGGTGT[A/G]CTGGGGTGTAGGGAT | 79058 |
rs113798932 | snp | C/T | 0.00993419 | 0.0697739 | downstream-variant-500B, intron-variant, missense | ASPSCR1 | GRCh38.p7 | 17:82017531 | GAGGAGCCTGGTGGA[C/T]CGTGGTGTGCATCCT | 79058 |
rs113917996 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016148 | CGCCAGGACCCGCCA[C/T]GCCTGGCCCCACCTT | 79058 |
rs113920236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995376 | GGCTGGGGCTGTGAC[A/G]GGGAGGTTCAGGTCT | 79058 |
rs113965270 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983446 | CAGGACGTGGATGGC[A/G]GGGCGTGGATGGCGG | 79058 |
rs113973567 | snp | A/G | 0.146985 | 0.227789 | upstream-variant-2KB, downstream-variant-500B | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81975573 | CTACCTCAGTGTCCC[A/G]AATAGCTGGGATTAC | 79058 |
rs114077868 | snp | A/C/G/T | 0.0140304 | 0.0825934 | utr-variant-3-prime, nc-transcript-variant, missense | ASPSCR1 | GRCh38.p7 | 17:82017345 | CAGCCTGAGGTGCCC[A/C/G/T]CTCCGCCAGCCACAG | 79058 |
rs114140681 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004964 | CAGCTGCTCCCATGG[A/G]CCTGCGACCTGCTGC | 79058 |
rs114165842 | snp | A/G | 0.00398564 | 0.0444627 | downstream-variant-500B, intron-variant, utr-variant-3-prime | ASPSCR1 | GRCh38.p7 | 17:82017855 | CTTTCAAACTGACCT[A/G]CTGAGGTGGGCAGGG | 79058 |
rs114314228 | snp | A/C | 0.0429648 | 0.14013 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994259 | GTCCGACATGGACTT[A/C]TAAGCACGGCCTCCC | 79058 |
rs114341171 | snp | C/G | 0.0905309 | 0.192535 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989362 | CCTGGTGGGCTCTCT[C/G]CTGGGAGCTGGTCCC | 79058 |
rs114569796 | snp | A/G | 0.0930568 | 0.194599 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008527 | TTGCTGTTGATGCCA[A/G]TTAGGGGTGACGCTG | 79058 |
rs114775497 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993159 | CACCTTGGGCTTTTC[C/T]GCTTGGTCTGTTCTC | 79058 |
rs114900274 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005247 | GTGGCAGGGTGGGGC[A/G]CCGGGGTGGCGGAAA | 79058 |
rs115007757 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995629 | AGGAATGGCCACCCC[C/T]GTGGGTGACAGCACG | 79058 |
rs115022010 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993082 | AAACAAAAGAAAACA[C/T]GTCAAACCCACACAC | 79058 |
rs115108602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986961 | AGATGGCAGCGGGTT[A/G]AGCACGAGCACGGAA | 79058 |
rs115138014 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991976 | TAAAGAATATGCCCT[C/G]GAAGCCAGCAGCAGA | 79058 |
rs115211119 | snp | C/G | 0.0402882 | 0.136092 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001897 | CACAGTGACACACGC[C/G]TGCCACACCGTAACG | 79058 |
rs115284731 | snp | A/G | 0.00213541 | 0.0326059 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994977 | CTCCAGGGCAGTGGC[A/G]GGAGACTCGGGCTCT | 79058 |
rs115487722 | snp | A/G | 0.10237 | 0.201756 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992289 | GCTGGAATTTCCCCC[A/G]GGCCCTGGCGTCCTG | 79058 |
rs115489649 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016097 | GGGATACCCCAGCCT[A/G]GCAGCTGCACCCCTC | 79058 |
rs115539223 | snp | G/T | 0.0715223 | 0.175059 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014703 | AGGGGGCGGCCAGGC[G/T]CTGGGCCACGTGTGC | 79058 |
rs115549610 | snp | A/G/T | 0.0463947 | 0.145069 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989728 | GTGTCACTGTAGCAC[A/G/T]CAGCCCTGGCCCGAC | 79058 |
rs115570592 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004141 | CTCTGGGCAGTGTCC[C/T]GGCCTGTGTGCATGC | 79058 |
rs115572094 | snp | A/C | 0.096524 | 0.197345 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997827 | TTTACTGAGGCACCC[A/C]CTTTTTTTTTTTTTT | 79058 |
rs115610076 | snp | C/T | 0.0919752 | 0.193722 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000468 | GCCGCCAGCCGCACA[C/T]GCAGAGGGCCCGGGG | 79058 |
rs115633099 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004281 | CTGCCCCCGGCATCC[C/T]GGACAGCGTCCCTGT | 79058 |
rs115648781 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985229 | ACAACTGCACACCCC[C/T]GCACACACCCACACA | 79058 |
rs115726428 | snp | C/G | 0.0655868 | 0.168795 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016071 | GGGAGGGGGAATCTG[C/G]AGCTGGGAGGGGGAT | 79058 |
rs115788781 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005551 | GGACACCTGGCGGCC[A/G]CACACCTGGGGGACC | 79058 |
rs115790730 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013946 | AGGTCACCCTGGGCT[A/G]GGCCCACCTTTGATG | 79058 |
rs115859818 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988939 | CAGGCCGGGCATGGC[A/G]GCTCTCACCTGTAAT | 79058 |
rs115881057 | snp | C/T | 0.0182019 | 0.0936463 | downstream-variant-500B, intron-variant, utr-variant-3-prime | ASPSCR1 | GRCh38.p7 | 17:82017825 | AAGTCTGATGACTTC[C/T]ACAGGCTCCCAGGGC | 79058 |
rs115893225 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995188 | CCGAGTGTGGCGTGG[C/T]GCAAGCAAAGCCCGC | 79058 |
rs115950133 | snp | C/G | 0.0356815 | 0.128715 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008760 | CCAGGGGCCATGTGC[C/G]CTGCTGGGGAGCAGG | 79058 |
rs116024081 | snp | A/G | 0.0916144 | 0.193427 | intron-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009290 | CCAGCACTGGCTCCC[A/G]GCCCAGGTCCCTGAC | 79058 |
rs116029752 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003744 | CACGCCGGTCGCAGC[A/G]GTCTCCCCACAGAGC | 79058 |
rs116069616 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990926 | ACGAGGGCAGGCGGG[C/T]GAGTCCCGTAGTTTG | 79058 |
rs116096769 | snp | A/G | 0.229786 | 0.249181 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995040 | GAGTGGCCGGCCCTC[A/G]GAGCCCGGGCTGCCC | 79058 |
rs116106717 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014713 | CAGGCGCTGGGCCAC[A/G]TGTGCATGCAGCCCC | 79058 |
rs116149334 | snp | A/G | 0.0669843 | 0.170309 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81994824 | CTCTCCTCCCAGGGA[A/G]TGCCTGCAGCACCCC | 79058 |
rs116268481 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991053 | ACTGTTGTGGGTGAC[C/T]GAGACCTGCCGTGGA | 79058 |
rs116428535 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013567 | GCAGGCGGCGGGCGC[A/G]GAAGCACCAGCTTTC | 79058 |
rs116636257 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000026 | TCCTCCCTCTGGGAA[C/T]TCTGCCAAACTCTGC | 79058 |
rs116720499 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008506 | GGCCCGGCTTTGTCA[A/G]TTTCATTGCTGTTGA | 79058 |
rs116845877 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985000 | TGCGTGCACACCCCC[A/C]CACACACCTGCACAC | 79058 |
rs116994706 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993221 | TGTTTTGTTTTGTTT[C/T]GTTTGTGTTTGAGAC | 79058 |
rs117194405 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997418 | CTGGAATCAAGCCCC[A/G]CCTCCTACCTGAGCA | 79058 |
rs117380711 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994276 | AAGCACGGCCTCCCC[A/G]GCCACAGGCAAGCGG | 79058 |
rs117386560 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006103 | TGTGTGCTTGGGGGC[A/G]TGTGTGTGTCCTTGC | 79058 |
rs117409128 | snp | A/C | 0.0115311 | 0.0750506 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994908 | CTTGCTCACCCAGTC[A/C]CCGCTCACTTTCAGC | 79058 |
rs117574737 | snp | A/C | 0.0471551 | 0.14613 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992184 | CCTGGCCTGGGGTCC[A/C]CGGGAGGCCCTGGGT | 79058 |
rs117733742 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994158 | TCAGGCATGTGTGGG[A/G]GGCGTGCTGCATATA | 79058 |
rs117832467 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999347 | ATTTGTGTCTGGGCC[C/T]GTGGCATGGTGGCTC | 79058 |
rs117835474 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992700 | CGGGTTCTGCTCCGG[C/T]GCATTTTGAGGCCTT | 79058 |
rs117874412 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986166 | CACAGTGGCTGGGCA[A/C]AGTGGCTTGCACTTT | 79058 |
rs117953264 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007488 | CCTTGGCACTGTCCA[A/G]TATGCGGACGTGGCA | 79058 |
rs118040910 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991929 | CGCGCCTTGCCGGAG[C/T]GGGGCCCCAGCGGGG | 79058 |
rs118150363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985149 | ACACGCACATCTGCA[C/T]GCACATGCGCACACC | 79058 |
rs137876848 | snp | A/G | 6.43687e-05 | 0.00567276 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996048 | GCTGGGCCTGACCGG[A/G]GGCAGCGCCACCATC | 79058 |
rs137948411 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013414 | TTCCCTACCAGCCAC[C/T]GTCTCCTGCCCTCCA | 79058 |
rs137954701 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976643 | TCCCCCTTCCACAGG[A/C]TACTGGGCAGCTGAG | 79058 |
rs137976141 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant, splice-acceptor-variant | ASPSCR1 | GRCh38.p7 | 17:81982613 | CTCTTAATTCTTCCA[C/G]ATGCCCCTGGGCTGT | 79058 |
rs138098095 | snp | G/T | 0.0463947 | 0.145069 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006080 | GTGCGTGTCCTTGCG[G/T]GTGCACGTGTGTGCT | 79058 |
rs138190996 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81979578 | TTGGATAATCTAGAA[C/T]GATTTATCATTACAT | 79058 |
rs138231466 | snp | A/G/T | 0.00557542 | 0.0525036 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999602 | ACTGCACTCCAGCCC[A/G/T]GGTGACAGAGTGAAA | 79058 |
rs138312789 | snp | A/G | 0.0170251 | 0.090679 | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81975843 | ATCTCAGCTCACTGC[A/G]AGCTCTGCCTCCCGG | 79058 |
rs138433775 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013822 | GGGAACAAAGCCCCC[C/T]GCCCCTGCCTGAAAC | 79058 |
rs138448677 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985144 | CACACACACGCACAT[C/T]TGCACGCACATGCGC | 79058 |
rs138477498 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81979905 | AGAAGGGTCAGAGCC[C/T]TCATATGGATAGGAT | 79058 |
rs138532070 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990741 | CTCCTGGAGGCACCC[A/G]GAGGAGGAAAGGGAG | 79058 |
rs138575918 | snp | A/C | 0.0189856 | 0.0955633 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987268 | GGAGTGGCGCCGGGC[A/C]GGGAGGCAGGCAGCC | 79058 |
rs138653497 | snp | C/T | 0.00438332 | 0.0466095 | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976200 | TCATGGCCACGCTGA[C/T]GTCCTGCACCTCCTG | 79058 |
rs138713176 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000081 | AGCGCTCGTGCCCCT[C/T]GACCCGTGTGCTCCG | 79058 |
rs138718591 | snp | A/G | 0.000242135 | 0.0110004 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996505 | CAGGCAGCCGCCAGC[A/G]CTCCACTTCCCTTGG | 79058 |
rs138723012 | snp | C/T | 0.000168455 | 0.00917601 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82016852 | CTCCCCATCTGCGGC[C/T]GATGTGCTGGTGGCC | 79058 |
rs138792224 | in-del | -/GGGCTCCGGGATGAGGCCGTGT | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997126 | GGATGAGGCCGTGTG[-/GGGCTCCGGGATGAGGCCGTGT]GGCTCCGGGATGAGG | 79058 |
rs138854615 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004986 | ACCTGCTGCCCGGGG[C/T]CGGGGGTCTGGGCCT | 79058 |
rs138862310 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990496 | CTGTGTCTGAGTTTG[A/G]GATCTTCCACGCCGA | 79058 |
rs138982807 | snp | A/G | 9.74516e-05 | 0.00697971 | downstream-variant-500B, intron-variant, missense | ASPSCR1 | GRCh38.p7 | 17:82017447 | AAAAGGGCCCCCGTC[A/G]TCTGCCCTGGCTCAG | 79058 |
rs139064158 | snp | C/T | 0.00260507 | 0.0359965 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996018 | AGCTGCCCTGCGGGG[C/T]ACGACGCTGCAGTCG | 79058 |
rs139082197 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994252 | TGGCAGAGTCCGACA[C/T]GGACTTATAAGCACG | 79058 |
rs139148000 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991102 | CGTGGGAACTCACAC[A/G]GCAGCTGAGCCGCTT | 79058 |
rs139199708 | snp | C/T | 0.000398116 | 0.0141032 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81985510 | TATACCCTCCAGGTT[C/T]GCATCGCTTTGCAGC | 79058 |
rs139291803 | snp | G/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983480 | GTGGATGGTGGGACG[G/T]GGATGGCGGGGCGTG | 79058 |
rs139415779 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007098 | ACGCCATATGTTCTC[A/G]GGGTGACTCAGGTGG | 79058 |
rs139515918 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002142 | TGCAGGTGTGAGCCA[C/T]TGCACCTGGCCTCTT | 79058 |
rs139526085 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006472 | ACTGTTGTGTCTGCC[C/T]ATCTTTCTGTGGGCT | 79058 |
rs139741942 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81980936 | TTTGGGTGCCCGAGG[C/T]GGAGGATTGCCTGAG | 79058 |
rs139761958 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982806 | TCTTTTCTTTTCTTT[C/T]CTTTCCTTTCCTTTC | 79058 |
rs139776731 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981098 | CAGAACCACTCCATG[A/G]TTGGTGGTTTCTTAT | 79058 |
rs139956530 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992231 | TTGGGACTTGCAGAG[G/T]TCTGCGTGGGGGAGG | 79058 |
rs139962253 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985302 | CTCACATGCACACAC[A/G]CATGCTGGTGCAGCC | 79058 |
rs139974101 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995602 | ATCCCTGCCCACCCC[A/G]AGCTGAGCACCAGGA | 79058 |
rs139989518 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985696 | TCAGAGCTGGACACC[C/G]AAGCTCTGTGCTGGC | 79058 |
rs139997963 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978611 | CGACTCGGAGTTTGC[A/G]GGAGCAGCCCACGGC | 79058 |
rs140163497 | snp | A/G | 0.0908922 | 0.192833 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010341 | GAGACCATCCTGGCT[A/G]ACACGGTGAAACCCC | 79058 |
rs140182235 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014872 | CAGCTAGGGAGGGGC[C/T]GGCTCCAGGCCCTCA | 79058 |
rs140270195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990461 | TCTGGGGGACACTGC[C/T]CTCCGCCTGCCTGGT | 79058 |
rs140291244 | snp | G/T | 0.00591614 | 0.0540654 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81979262 | TGCTCCAGCTCAGCA[G/T]CAGGGTCTGAGTATA | 79058 |
rs140358565 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005076 | TGCCCCGGCAGCCGT[A/G]GGGCTCTCGCCTCTG | 79058 |
rs140464637 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999041 | TGACCCCGCATCAGA[A/G]CCCTGCACCTGGGCT | 79058 |
rs140516312 | in-del | -/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984994 | ACACCTGCGTGCACA[-/C]ACCCCCCCACACACC | 79058 |
rs140557125 | snp | A/G | 0.0452528 | 0.143452 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978740 | GCGGGACCCCTTGGT[A/G]CAAGGCCACGGCTTT | 79058 |
rs140583012 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008476 | AATCACTGCCCAGGG[A/C]TCCGCGAGCTGCACG | 79058 |
rs140833927 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990200 | CACGTAGTCAGTAGA[A/G]AAGTGAGCCGTCTCA | 79058 |
rs140840218 | in-del | -/T | | | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81975761 | CTGGCCATATTTAAT[-/T]TTTTTTTTTTTTTTT | 79058 |
rs140843585 | snp | A/G | 0.0479149 | 0.147179 | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81975857 | CGAGCTCTGCCTCCC[A/G]GATTCACGCCATTCT | 79058 |
rs140950477 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002835 | ATTGTTAGGATTACA[A/G]GCGTGAGCCACCGCG | 79058 |
rs141150374 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982486 | TCCAAGGTTCCCAGC[C/T]TGCCTGCCCTCGGGA | 79058 |
rs141177595 | in-del | -/GGG | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000166 | AGAGACACAGTGGCT[-/GGG]GTCATGTTCCCCCAT | 79058 |
rs141208381 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003999 | GGGAGGGAGGGAGGC[C/T]GGGAGGGAAAAACAC | 79058 |
rs141245984 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007634 | ACTCTGCCCGCCTGG[C/G]AAGACAGTGTGGCTT | 79058 |
rs141296467 | snp | C/G/T | 0.000116489 | 0.00763107 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82010829 | GTCCTGTTCCCCGAC[C/G/T]GCTACGTCCTACAGG | 79058 |
rs141323909 | snp | A/G | 0.000102504 | 0.00715832 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016780 | TCAGAGGCTCAGGGT[A/G]AGCTTGGGCCTCCCT | 79058 |
rs141363920 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987327 | AGCAGGGATCCCGGC[A/G]CCCTGGCTCTGTGCT | 79058 |
rs141391086 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012651 | GGAGCAGGGCTCAGG[A/G]AGCCCCAGAGGGACC | 79058 |
rs141442327 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991288 | GGCTGGATCTCTTCC[C/T]AGGCCCCCAGCCCTC | 79058 |
rs141636229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001622 | CCACTGGGGCTGTGG[A/G]GAGAACTGGGAGTGT | 79058 |
rs141708885 | snp | C/G | 0.0045751 | 0.047609 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994964 | GTCCCGCAGCCGTCT[C/G]CAGGGCAGTGGCGGG | 79058 |
rs141743833 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995453 | CAGCACTGTCCTGAG[G/T]CTGTGGCCCTCAGGG | 79058 |
rs141833216 | snp | A/T | 0.0207231 | 0.09966 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010102 | GTTTTTTTTTTTTTT[A/T]CTAGAGATGGAGTTT | 79058 |
rs141934232 | snp | G/T | 0.0618563 | 0.164627 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010187 | TCGGCCTCCCAAAGT[G/T]CTGGGATTACAGGCT | 79058 |
rs142162975 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982754 | GTTTTCTCTTTCTTT[C/T]TTTCTTTCTTCTTCT | 79058 |
rs142203224 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015000 | GAGAGGCCCCTCAGC[C/T]TGTGCCTCCCTCAAA | 79058 |
rs142237607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982262 | GCATGAGCCACCGCG[C/T]CCAGCGCATTGTTAC | 79058 |
rs142278915 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983732 | CAGCTGGCCAGGGAC[A/G]GGGGACGGGACAGTG | 79058 |
rs142400444 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81980669 | TGGAAACAGACACTT[C/G]AAGAGAGGGAAGAAT | 79058 |
rs142417799 | in-del | -/C | 0.0456336 | 0.143994 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984828 | GCACACCCGTACACA[-/C]CCCCACACACCCCTG | 79058 |
rs142531286 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81998159 | TATTTTTCATAAAGA[C/T]GAGGTCTCTCTCTGT | 79058 |
rs142584577 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992591 | GACCCCTGGCCATCT[G/T]TGTCATGCTGGGGAG | 79058 |
rs142607745 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993754 | CAAGCAGTTTCCAGC[C/T]CAGCTGTTACCTAAT | 79058 |
rs142687226 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006370 | GTATATGCATGTCTG[C/T]GTGTGCACATATGTG | 79058 |
rs142739617 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989998 | GTTTCACCATGTTGG[C/T]CAGGCTGGTCAGGTG | 79058 |
rs142782896 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016039 | CCCCAGCCTGTGGCC[C/T]TGAGCAGCCTGGAGC | 79058 |
rs142793412 | in-del | -/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007936 | TCAGCCACCTGTGGG[-/C]CCCCACTGCCGAGCC | 79058 |
rs142800936 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003425 | TGCACTCCAGCCTGG[A/G]CAACAGAGCGAGACG | 79058 |
rs142841603 | snp | A/G | 5.18121e-05 | 0.00508954 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996539 | CTGGGGAGCTCAGCC[A/G]CGGCGACTTGAGCCG | 79058 |
rs143008575 | snp | A/G | 0.00177739 | 0.0297579 | splice-acceptor-variant | ASPSCR1 | GRCh38.p7 | 17:82016939 | TCTTCGCCTCCCCAC[A/G]GGTACATGTCCAGGG | 79058 |
rs143135376 | snp | C/T | 0.00118665 | 0.0243293 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81979134 | CTGGCCCACTGCGCC[C/T]GCCAGCCCTGCACAC | 79058 |
rs143140087 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990321 | TCCACTCTGCTTCTC[A/G]GGCTCTGCTGCAGGG | 79058 |
rs143151494 | in-del | -/GT | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006180 | CACGTGTGTGCACGG[-/GT]GTGTGTGTGTGCGTC | 79058 |
rs143182864 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992315 | TCCTGCACACTGGGC[C/T]GGCGTAGAAGGTCTG | 79058 |
rs143225273 | in-del | -/TGCC | 0.0521331 | 0.152803 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013479 | GTGTCCCCGGTGACG[-/TGCC]TGCCTGCCTGCCTGC | 79058 |
rs143326652 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987528 | TCCCTGGCTGTGCTG[C/T]CAGTCCTCAGATGGG | 79058 |
rs143435714 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984873 | ACACCTGCACACCCC[C/T]GCACACACACCCCCC | 79058 |
rs143551347 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009393 | GGAGAGCAGCCCACT[C/T]CCACCCTGGAGGGTG | 79058 |
rs143611162 | snp | A/G | 0.130351 | 0.219509 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010357 | ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 79058 |
rs143807418 | snp | A/G | 1.66457e-05 | 0.00288489 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82010833 | TGTTCCCCGACCGCT[A/G]CGTCCTACAGGGCTT | 79058 |
rs143827048 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988448 | TGACAAAGCAGGACT[C/T]CGTCTCAAAAAAAAA | 79058 |
rs143832979 | snp | C/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82012259 | AAAAACAGTCCTGGA[C/G]GACCACACGCAGACC | 79058 |
rs143841140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990722 | GCCCTGGGGGTACAC[A/G]GCCCTCCTGGAGGCA | 79058 |
rs143876559 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006090 | TTGCGTGTGCACGTG[C/T]GTGCTTGGGGGCGTG | 79058 |
rs143947080 | snp | C/G | 0.154344 | 0.230976 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010028 | GGTTCTCCTGCCTCA[C/G]CCTCCCAAGTAGCTG | 79058 |
rs144189258 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978818 | AGGTGCACAGAACCG[C/T]GCCAGAGCCAGGGGG | 79058 |
rs144193916 | snp | C/T | 0.00534541 | 0.0514211 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82009084 | GGTGGTGTGCCACCC[C/T]GACCTGGAGGAGCGG | 79058 |
rs144209431 | snp | A/G | 0.0456336 | 0.143994 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81980937 | TTGGGTGCCCGAGGC[A/G]GAGGATTGCCTGAGC | 79058 |
rs144302246 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81998303 | AATATTGTGGATAGT[A/G]TCATGCTTCCTGTTA | 79058 |
rs144352355 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002504 | AGGTGATCCACTTGC[A/G]TCGGCCTCCCAAAGT | 79058 |
rs144388157 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983205 | TGACACTCCAGCTTC[C/T]GCGAGTGCAGCAGTG | 79058 |
rs144395852 | snp | C/T | 7.44158e-05 | 0.00609938 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81983640 | AGATGGTGCCCGCTT[C/T]CCGGAGCCGTGAGGG | 79058 |
rs144440213 | in-del | -/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003376 | TGCCTGAGCCTGAGA[-/T]GATCAAGACTGCAGT | 79058 |
rs144524715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989939 | ATTACTGGCGCACGC[C/T]ATCACGCCTGGCTAA | 79058 |
rs144660143 | snp | A/G/T | 0.00700384 | 0.0587618 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81985539 | GCTGGACGATGGCTC[A/G/T]AGGTTGCAGGACTCT | 79058 |
rs144787705 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999939 | CCTGGGACTGTTCCT[A/G]TTGAGTGGACAAGGG | 79058 |
rs144807549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002866 | CCCGGCCTGTTTTCA[C/T]CTTTTTAAAATAACT | 79058 |
rs144846209 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006725 | CCTGCAGGGCCCTCG[C/T]TGTCGCTTTTTTCCC | 79058 |
rs144867148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987009 | GAACTCAGACAACAG[C/T]GACGGAGCCTAAGAG | 79058 |
rs145080338 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004417 | CTGGAGGCCGGGACC[C/T]GGGGGTCCACCGGGG | 79058 |
rs145112942 | snp | C/T | 8.38497e-05 | 0.0064744 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82017287 | CGGGGTGTGTGGTCA[C/T]CCTGATGTGTCTGCA | 79058 |
rs145237583 | snp | C/T | 0.00100815 | 0.022429 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011657 | TGCTCGGGGCCTTGG[C/T]GCTGTGGGCACACCG | 79058 |
rs145405538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007222 | GTGTGGGAGGTTTCC[A/G]TAGAGGCCGCTCTCC | 79058 |
rs145575872 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997367 | TGGCCAGGGAAGGGG[C/G]AGCTGGTGAACGCAT | 79058 |
rs145675837 | snp | C/T | 0.000314932 | 0.0125446 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81985555 | AGGTTGCAGGACTCT[C/T]TCTGTTCAGGCCAGA | 79058 |
rs145684585 | snp | A/G | 0.000546869 | 0.0165268 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81985528 | ATCGCTTTGCAGCTG[A/G]ACGATGGCTCGAGGT | 79058 |
rs145755880 | snp | A/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981677 | AGTCACTGTGCCTGG[A/C]CATTTTTCTGAAACA | 79058 |
rs145777966 | snp | A/G | 0.00636936 | 0.0560724 | | | GRCh38.p7 | 17:81982298 | AGTGTTCACCTGCCC[A/G]TGGTCTGTGTGGTGG | 79058 |
rs145797114 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985113 | ACATACCCGCACACA[C/T]CTGCATGTAAACATG | 79058 |
rs145874774 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002977 | CCTCCTGGGTTCAAG[C/T]GATTTTCGTGTCTCA | 79058 |
rs145991424 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995569 | AGTTAGCGTATGGGA[C/T]GTGGCCAGCCAGGCC | 79058 |
rs146038640 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992098 | TACCCTGCTGCGAGC[A/C]GGCACCCGCGGAAGC | 79058 |
rs146112942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014597 | CGCCTCCCTCCCAGG[C/T]GCTGTGGTGCCGCCT | 79058 |
rs146269701 | snp | A/G | 0.000461474 | 0.015183 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995960 | TGGGGTCCCGGTGCA[A/G]GGCGCACCTGTCCTG | 79058 |
rs146351637 | snp | G/T | 0.0528381 | 0.153711 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982793 | TTTTCTTCCTTTCTC[G/T]TTTCTTTTCTTTTCT | 79058 |
rs146387239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994217 | TGCCTCCTGCGGGGC[A/G]AGGCTCAGAAAGACA | 79058 |
rs146404268 | snp | C/T | 0.00755907 | 0.0610114 | downstream-variant-500B, intron-variant, utr-variant-3-prime | ASPSCR1 | GRCh38.p7 | 17:82017720 | CCCACATCCGTAGGG[C/T]AGGGCCTGGCCTCAG | 79058 |
rs146404359 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81980714 | CACCGAATGGGGTGG[C/G]TGATACAGACGTACT | 79058 |
rs146513986 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990058 | GAGATTACAGGCGTG[A/C]GCCACCACACCTGGC | 79058 |
rs146534465 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981065 | ATGAAGACTGTGCCA[C/T]GAAAACCCTGACTGT | 79058 |
rs146550986 | in-del | -/CCGTGTGGGCTCCGGGATGAGG/CCGTGTGGGCTCCGGGATGAGT | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997119 | CGCTCCGGGATGAGG[lengthTooLong]CCGTGTGGGCTCCGG | 79058 |
rs146589185 | snp | A/G | 2.21594e-05 | 0.00332855 | missense, nc-transcript-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009164 | TGGACGACGTGAGAA[A/G]ACGCTTGGCCCAGCT | 79058 |
rs146652909 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992331 | GGCGTAGAAGGTCTG[C/G]AACCGATTGCCCACC | 79058 |
rs146820629 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008096 | CGAGGTCTCAGGTGT[A/G]TCCGGAGGGCAGCCC | 79058 |
rs146933568 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013169 | CCTGCAGCGGAGGCA[A/G]GGGAGGGGTGAGACA | 79058 |
rs146977810 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982054 | GCACACTGCAACCTC[C/T]GCCTCCCGGGTTGAA | 79058 |
rs147020746 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81979511 | TTCTTGTGGCCTTTT[A/C]CTGTTTTCTCTGTGT | 79058 |
rs147036198 | in-del | -/TG | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006219 | GTGCACAGGTGTGTG[-/TG]TGTGTGTGTGTCCTT | 79058 |
rs147132825 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81979858 | TTCCCAAGAGAGGGC[C/T]TCTGCCAGACTCTCA | 79058 |
rs147176021 | snp | C/T | 0.000243081 | 0.0110219 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996482 | TGGGCTCGTCAGCGT[C/T]GGCTGGCCAGGCAGC | 79058 |
rs147198825 | snp | C/G/T | 0.000263593 | 0.0114774 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81979202 | CTGGAGGACACGTGC[C/G/T]GGCGGCAGGACTTCA | 79058 |
rs147238722 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990812 | ATGCTAACGGGTTTC[C/T]TATGAGGAGTTTCTC | 79058 |
rs147272065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986192 | ACTTTGGAAGGCCGA[A/G]GCTGGCGAATCGCTT | 79058 |
rs147316194 | in-del | -/T | 0.0475351 | 0.146656 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984626 | ATCTCATGTGGCTTC[-/T]TGAGGGTCAGGAATC | 79058 |
rs147352955 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976586 | GTGGCTCACGTGTGT[A/G]ATCCCAGCCCTGTGG | 79058 |
rs147378393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002825 | GGCCTCCCAAATTGT[C/T]AGGATTACAGGCGTG | 79058 |
rs147387984 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006399 | TGCATGCATGTTTGC[C/G]CCAGAGCGGAAGGAA | 79058 |
rs147391651 | snp | C/T | 3.45316e-05 | 0.00415507 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996543 | GGAGCTCAGCCGCGG[C/T]GACTTGAGCCGTCCG | 79058 |
rs147635421 | snp | C/T | 0.00301653 | 0.0387191 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82016848 | CCATCTCCCCATCTG[C/T]GGCCGATGTGCTGGT | 79058 |
rs147647132 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982081 | TGAAGCACTCCTCCC[A/G]CTTCAGCCTCCCGAG | 79058 |
rs147748741 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993505 | GGCGTGAGCCACCGC[A/G]CCCGGCTGAGTCCTG | 79058 |
rs147813785 | snp | C/G/T | 0.000398466 | 0.0141104 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016555 | GGTTGGGGCCAGTGT[C/G/T]GGAGTCCAGCCAGCC | 79058 |
rs147861765 | snp | G/T | 0.0312537 | 0.121037 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81983668 | GGGGCCTGAGAACAT[G/T]GTGGGTCGTGCTCTG | 79058 |
rs148022587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009428 | TGAGGAGCCCGGGGC[C/T]TGTTGCCAGGGCCCC | 79058 |
rs148055909 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001331 | CCCCACATCCGACGC[A/G]GTGCAGACTCCCATC | 79058 |
rs148162287 | snp | A/G | 1.66095e-05 | 0.00288175 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82012268 | CCTGGACGACCACAC[A/G]CAGACCCTCTTTCAG | 79058 |
rs148225721 | snp | A/G | 0.000310875 | 0.0124636 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82017028 | TGCTGAGGAGGGGGC[A/G]CTGGTCCCCCCTGAG | 79058 |
rs148233930 | snp | A/G | 0.000758362 | 0.0194578 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81979135 | TGGCCCACTGCGCCC[A/G]CCAGCCCTGCACACT | 79058 |
rs148380776 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987609 | GGGCCGAGGGTGTCT[A/G]GAGAGGTGGGGCCGG | 79058 |
rs148388407 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015558 | GCCTCTCTGCATCGG[-/T]TGGCCTCTGAGGGAG | 79058 |
rs148431560 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992399 | ATCCCTCTGGAGGAG[C/G]CGCACATCAAAGCCG | 79058 |
rs148481986 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989953 | CCATCACGCCTGGCT[A/G]ATTTTTGTATTTTTT | 79058 |
rs148483554 | snp | A/G | 5.0885e-05 | 0.0050438 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996625 | AGCACAAGGGCACCC[A/G]CAGCTGCCCCCTTTG | 79058 |
rs148572120 | snp | A/G | 0.00180799 | 0.0300121 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010059 | GGATTTCAGGTACCC[A/G]CTACCACTAGCTCGG | 79058 |
rs148628387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997346 | GGGGTGGTAACTTCC[A/G]GGTTATGGCCAGGGA | 79058 |
rs148727843 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983235 | GTTCACGCCCCAGTC[A/G]TTCTCTCTGTGTTTT | 79058 |
rs148783566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81980369 | GCCCACCCTGCCTTA[C/T]GAGGCTCTCCTGGGA | 79058 |
rs148833846 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983979 | TCTGCCTCAGCCTCC[A/C]GAGTAGCTAGGACTA | 79058 |
rs148885640 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981945 | TGCTGGGATGATAGG[C/T]GTGAGCCACTGCACC | 79058 |
rs148980532 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990580 | GATCTTCCACGCCGA[A/G]CTCTGGGGGACACTG | 79058 |
rs149000044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003024 | GGATTACAGGTGCCC[A/G]TTTAGTAGAGATGGA | 79058 |
rs149012488 | snp | A/G | 6.64805e-05 | 0.00576505 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82011555 | CAGTGGGGGACTTGC[A/G]AGACTTCGTGAGGAG | 79058 |
rs149041999 | snp | C/T | 0.0036495 | 0.0425609 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016928 | ACCACTCTGTGTCTT[C/T]GCCTCCCCACAGGTA | 79058 |
rs149095241 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012478 | CTTTCCGGCCTCCTC[A/T]GCTTCCTGCCTGGCC | 79058 |
rs149103743 | in-del | -/GT | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006301 | CGTGCGTGTTTGGGG[-/GT]GTGTGTGTGTCCTTG | 79058 |
rs149260970 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81979957 | GAAGCTTTTCACTTT[A/C]AAGTCCTGTTTTCTG | 79058 |
rs149312781 | snp | C/G | 0.0494327 | 0.149241 | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976577 | CCGGGTGCGGTGGCT[C/G]ACGTGTGTAATCCCA | 79058 |
rs149350280 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994310 | TGAGCGGAGTGCAGC[A/G]CCCCTCCCTCCATGC | 79058 |
rs149356314 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985395 | GGTCAGCCTCTCCCT[C/G]GAGGCCAGGGCGGGG | 79058 |
rs149452310 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996060 | CGGGGGCAGCGCCAC[C/T]ATCAGGTAAGGGCAG | 79058 |
rs149523512 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006087 | TCCTTGCGTGTGCAC[A/G]TGTGTGCTTGGGGGC | 79058 |
rs149576419 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999842 | GGGCAGAGGCCGGGC[A/G]TCTGCACCGTGTTGG | 79058 |
rs149618534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013910 | CTTCTGTGTGCGGTC[C/T]GCGTCCTCAGGTCAT | 79058 |
rs149720294 | snp | C/T | 0.00104779 | 0.0228648 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82016477 | CGCCCTCCCTGCAGG[C/T]GAACCTCTTCCCGGC | 79058 |
rs149725769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989519 | TCTTTCATGTGTTTC[A/G]GAGGAGGTCTGAGTC | 79058 |
rs149772045 | snp | A/G/T | 6.63587e-05 | 0.00575984 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81985511 | ATACCCTCCAGGTTC[A/G/T]CATCGCTTTGCAGCT | 79058 |
rs149810544 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981590 | CACCATGTTGGTCAT[G/T]CTGGTCTTCAAGTCC | 79058 |
rs149839652 | snp | A/G | 0.0236746 | 0.106192 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978638 | CGGCGTGGGGTCCCC[A/G]GGCCTGGGCAGGTGG | 79058 |
rs149872107 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81996330 | GGGAGAGGGTGAGCC[A/G]GGGGCGGGAGAGGGT | 79058 |
rs149880133 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986985 | CACGGAATTCTCCCT[C/T]CCAAAACGGAACTCA | 79058 |
rs150019630 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011469 | GGAGGGTGGGAGCAG[C/T]GGCCCAGGTGCTGGG | 79058 |
rs150072142 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007187 | CCGGATCGGGGCTGC[C/T]CTGCCCAGGTGAAGG | 79058 |
rs150121558 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013757 | GGGCTGGGAGGAGGC[A/G]GCCAGGAGTGAGGAC | 79058 |
rs150393924 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999279 | TTGAGCTCCTGCTGA[C/T]GTAGTGGGCCTGGAA | 79058 |
rs150701474 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985249 | ACACCCACACACACA[C/T]ATGCACACACGCACG | 79058 |
rs150701534 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010257 | CATTTGAGCCGGGCG[C/T]GGTGGCTCACGCCTG | 79058 |
rs150806011 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997451 | GTCACTGGGCTTGTT[C/T]TTAGCTTCTCAGGCA | 79058 |
rs150829995 | snp | C/T | 0.000436989 | 0.0147751 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996732 | GTTGCCGAAGTCCCT[C/T]TCCAGCCCTGGAGGC | 79058 |
rs150865619 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007084 | CAGCCCTACTGCAGA[C/T]GCCATATGTTCTCGG | 79058 |
rs151025812 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003884 | TCGGGAGGTTTGGCC[C/T]GTGTCTGGCGTAGTG | 79058 |
rs151067786 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016414 | CTGGGGGTGTAGCTG[C/T]CTTCACAGCAGGGGG | 79058 |
rs151281652 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983412 | CAGGTCATGACGTCC[C/T]GCTGTTGGGGAGCTG | 79058 |
rs180819306 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995178 | ATTTTCAAAACCGAG[G/T]GTGGCGTGGCGCAAG | 79058 |
rs180828348 | snp | A/G | 0.00755907 | 0.0610114 | downstream-variant-500B, intron-variant, utr-variant-3-prime | ASPSCR1 | GRCh38.p7 | 17:82017678 | CAAGCCCTGGGCCAG[A/G]AGCTGGGGGAGGAGC | 79058 |
rs180834917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008856 | GTGGGGTGGGGTCCC[C/T]CAGCTGCTGTGCCCA | 79058 |
rs180860316 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988548 | GGTGGTAAAGCCCGG[A/G]GCCCCCAGCCTGCGG | 79058 |
rs180879213 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992186 | TGGCCTGGGGTCCCC[A/G]GGAGGCCCTGGGTCT | 79058 |
rs180888881 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983172 | TGTGGTGGCTCCAGC[C/T]GTGACGGCCGGGGTC | 79058 |
rs180924216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011721 | ACAGGAGCAGCATCT[A/G]TGGCCTCCCGCCCAG | 79058 |
rs180953727 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001982 | TGTTCTTATTTTTCT[A/T]TTCTTTTTTTTTTCT | 79058 |
rs181139818 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988318 | ATACAAAAATTAGCT[C/G]GGCGCAATGGCTCAT | 79058 |
rs181380192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008167 | CTGGCTGTCACCCAG[C/T]GTGGGCATGGTGGGG | 79058 |
rs181584718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | ASPSCR1 | GRCh38.p7 | 17:81982617 | TAATTCTTCCAGATG[C/T]CCCTGGGCTGTCTGA | 79058 |
rs181591043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990897 | GGGGATACTGTAGCA[C/T]GTCTGGGCAGTCCAC | 79058 |
rs181623501 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986250 | GCAACATAGTGAAAC[C/G]CCTTCTCTACAAAAA | 79058 |
rs181695835 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001152 | TTGGGGGTAAACCAG[A/C]GGGGAGGAGGCTGGG | 79058 |
rs181726751 | snp | A/G | 0.000120972 | 0.00777634 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996480 | CCTGGGCTCGTCAGC[A/G]TCGGCTGGCCAGGCA | 79058 |
rs181935597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006806 | TGAATCCACCTGGCG[C/T]GGGAGCGGCGCTGAT | 79058 |
rs181963342 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976495 | TGTGTGGGTGACATG[A/G]ATATGTCATCGACAG | 79058 |
rs181975075 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982199 | CTCTCAAACTCCTGA[C/T]CTCAAGTGATCTGCC | 79058 |
rs181993317 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012434 | GGTTCCGAGGGGGCC[A/C/G]TGCGCCTCTGAAGTT | 79058 |
rs182000229 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992387 | GGAGGGAATCTGATC[C/T]CTCTGGAGGAGCCGC | 79058 |
rs182127454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81998169 | AAAGACGAGGTCTCT[C/T]TCTGTTGCCCAGGCT | 79058 |
rs182246049 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000888 | GCTGGGCTGGGACGC[C/T]AGTCCCAGCAGACGC | 79058 |
rs182258946 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81979021 | TGCAGGTGAGAGCCT[A/G]CATTTGTTGCGGGGA | 79058 |
rs182621593 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989036 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 79058 |
rs182634886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010117 | ACTAGAGATGGAGTT[C/T]TACCATGTTGGCCCG | 79058 |
rs182654353 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993276 | TGGAGTGCAGTGGCG[C/T]GATCTCGGCTCACTG | 79058 |
rs182734871 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004792 | GGTCGGGAAGAAGGG[A/C]GTGTGGGGCCTTTGG | 79058 |
rs182748954 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984097 | ACCTCATGATCTACC[C/T]GCCTCGGCCTCCCAA | 79058 |
rs182858192 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013272 | GGCCAGCCAGTTGAT[A/G]AACATTGAATTTGGA | 79058 |
rs182906533 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014694 | TCTCGTTGGAGGGGG[C/T]GGCCAGGCGCTGGGC | 79058 |
rs182966848 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009727 | CACAGCTCTGAGCGG[A/G]CCCCCTGTGAGGTCT | 79058 |
rs182968062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988678 | TGACTGTTGTTGCTG[A/G]TGAATATGCTGTGGA | 79058 |
rs183128607 | snp | A/C | | | upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977433 | ATCCAAGCCGCGCTT[A/C]CCGGAGGCAGAGGAC | 79058 |
rs183403318 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997396 | ATCAGCCAGTCTTCA[A/G]TCTGGTCTGGAATCA | 79058 |
rs183460245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000063 | ACACCTGAGTCCCCA[C/T]GAAGCGCTCGTGCCC | 79058 |
rs183471512 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982003 | AGACGGAGTCTCGCT[C/T]TGTCGCCCAGGCTGG | 79058 |
rs183515194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81998755 | TCGAATTTCACCTGG[C/T]TCACAAGGGAGCTGG | 79058 |
rs183552212 | snp | A/G | 0.000161898 | 0.00899571 | missense, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015309 | CGTCCGAGCAGTGGC[A/G]ATCCCTCCCGAGTCA | 79058 |
rs183557822 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993415 | AGACGGGGTTTCATT[A/G]TGTTAGCCAGGATGG | 79058 |
rs183613928 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992972 | CCACGACCCTGTGGG[A/G]CCTCTGCAGCCAGAC | 79058 |
rs183664959 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005355 | CTCTTGCTGCCCTGC[A/G]GTTCAGTTCCTCCTG | 79058 |
rs183756791 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81980084 | ACCTCCTAGGTTCAA[A/G]TGATTCTCCTGCCTC | 79058 |
rs184011246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983408 | TCTGCAGGTCATGAC[A/G]TCCCGCTGTTGGGGA | 79058 |
rs184120981 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010346 | CATCCTGGCTGACAC[A/G]GTGAAACCCCATCTC | 79058 |
rs184156012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981102 | ACCACTCCATGGTTG[A/G]TGGTTTCTTATCAGG | 79058 |
rs184171970 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002464 | TTTGCCATGTTGGTC[A/T]GGCTGGTCTCGCACT | 79058 |
rs184276891 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989408 | AGGGAGGGAGGCTCT[C/T]GTGCCTAGTGTCCCT | 79058 |
rs184307006 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011367 | GGGGGTCCCAAGTGT[C/G]GCCCGCACGGTGGCC | 79058 |
rs184354145 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986653 | CCTCCCCGGGCCTCA[A/G]TTTCCTCACCTGTGC | 79058 |
rs184429880 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007017 | GTTTCTCCACACACA[C/G]GGTCCCCTGGCATCT | 79058 |
rs184591864 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990210 | GTAGAAAAGTGAGCC[A/G]TCTCATGCTCTTGTT | 79058 |
rs184696266 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994586 | AGCCCCCAGGCCACG[A/C]ACCACAGGCCAGGGT | 79058 |
rs184828379 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016599 | CAGAGCCAGCTGCCC[A/G]GGAGGGCGTTCGGTC | 79058 |
rs184842222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010671 | AAGCCCAGGCCCTGA[C/T]TGGGGGTGGCTGCTT | 79058 |
rs184940676 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991915 | CCCCAGCACACAGCC[G/T]CGCCTTGCCGGAGCG | 79058 |
rs184995296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015800 | TGGCTCCCCAGCTTC[C/T]GGCGCCTCTCCAGGG | 79058 |
rs185058927 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81998961 | TCACGCCTCCCCCCA[A/G]CCGTGGGGACCTCGT | 79058 |
rs185101157 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993991 | AGGAAGGCCTGAGAA[A/G]GGCTTTTGTTTTTCT | 79058 |
rs185182696 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002074 | GTGCAGGGGCACAAT[C/T]ACGGCTCACAGCAGT | 79058 |
rs185203702 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983225 | GTGCAGCAGTGTTCA[C/T]GCCCCAGTCGTTCTC | 79058 |
rs185493665 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000908 | CCAGCAGACGCCCCC[A/C]ACAACTCGGCCTCCC | 79058 |
rs185608572 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008412 | CGAGTGTGGGTCGGC[A/G]CAGTGCTGAGGTGTC | 79058 |
rs185610488 | snp | A/G | 0.0217236 | 0.101931 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977929 | CGCTGGGGTCCCGGG[A/G]GTCCCGGGGGTCCCG | 79058 |
rs185617864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997919 | GTAACCTCCACCTCC[C/T]GGGTTCAAGCGATTC | 79058 |
rs185732824 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986069 | TCAGCCTCCCAAAGC[A/G]TTGAGATTACAGGTG | 79058 |
rs185741354 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001661 | GTACTGGGCGAGTCG[A/G]CTGCTGCAGGGCGCA | 79058 |
rs185850059 | snp | A/G | 0.000487284 | 0.0156014 | intron-variant, missense | ASPSCR1 | GRCh38.p7 | 17:82012186 | GGCGCATGGATGGGC[A/G]AGGTCCACGGTGCTT | 79058 |
rs185850440 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982723 | TTTTCTTTTCTTTTC[C/T]TTCTTTTTCTTTCTT | 79058 |
rs185873835 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006670 | CGAGGAGGCTGGGGA[C/G]GGGGGACGGGAATTC | 79058 |
rs185980513 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992311 | GGCGTCCTGCACACT[G/T]GGCCGGCGTAGAAGG | 79058 |
rs186159033 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992494 | GCGGTCAGTGCCGGG[C/G]AAGGACTGTGAGTTG | 79058 |
rs186376955 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993066 | AAAAATAAAGGCCAC[A/G]AAACAAAAGAAAACA | 79058 |
rs186418945 | snp | G/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995287 | GCCCTTTGCTGGGGT[G/T]GGGGGGCACTGGCCC | 79058 |
rs186425713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988388 | TGAACCCGGGAGGCG[A/G]AGGTTGTAGTGAGCT | 79058 |
rs186426718 | snp | A/T | 0.00438332 | 0.0466095 | utr-variant-3-prime | ASPSCR1 | GRCh38.p7 | 17:82018019 | CAGGGGCAGCTTTTG[A/T]GCTTCCCACCCTGGG | 79058 |
rs186431524 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976286 | TGTGGGACAGTCTAA[G/T]GAAAATAGGAACAGA | 79058 |
rs186566857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014198 | CTGCTGGGCGCCCGC[C/T]CCTAGCCAGTTCTGT | 79058 |
rs186645659 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, splice-acceptor-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976959 | AAGTCCTTGAGTGCC[G/T]GTGGGTCGGCAGGAG | 79058 |
rs186771370 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005377 | TTCCTCCTGCTGCAG[C/T]GCCTGTGTGCCCCGT | 79058 |
rs186852466 | snp | C/T | 0.000172096 | 0.00927462 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996564 | GAGCCGTCCGGAGGA[C/T]GCGGACACCTCAGGG | 79058 |
rs187019689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004886 | GAAGGCACTGGTGTC[C/T]GGGGGCATCAGCGGC | 79058 |
rs187031998 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984483 | TCAGCAGGCTGAGGC[A/G]GGAGAATGGCGTGAA | 79058 |
rs187219243 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988562 | GAGCCCCCAGCCTGC[A/G]GCCCTGGTCTGTGTG | 79058 |
rs187261837 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010058 | GGGATTTCAGGTACC[C/T]GCTACCACTAGCTCG | 79058 |
rs187264821 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988753 | CTCTTCCGTCGTGTG[A/G/T]GTGTCATGTGGGTGT | 79058 |
rs187291970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982338 | GGAACCAGTGAGTGC[A/G]ATTTTGAGGCAGGTC | 79058 |
rs187437797 | snp | C/T | 0.0027224 | 0.0367939 | intron-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009224 | GCCTCCCGGCATCTT[C/T]GCGCCAGGGTTTGCC | 79058 |
rs187703368 | snp | G/T | 0.0463947 | 0.145069 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985969 | GGATGGGATCATAAG[G/T]TCTCTTTTTTTTAAG | 79058 |
rs187708792 | snp | C/T | 0.000949064 | 0.0217631 | stop-gained, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015225 | GGTCCATCCAGAGGC[C/T]GAGCCTCTCCAAGCA | 79058 |
rs187738018 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993358 | AGCTGGGACCACAGG[C/T]GCCCGCCACCACGCC | 79058 |
rs187846323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015528 | TGGCCTGTGGGGGCT[A/G]TGATGAGAACCAGGT | 79058 |
rs187860638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993726 | CAGTACCCCCCATCC[C/T]GGAGGGTTGCTGCAA | 79058 |
rs187912022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81998278 | ACCAGGCCTGAAAGT[C/T]ACTTTTTATAATATT | 79058 |
rs187925874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81979496 | CTCTCTGCCTCCGAT[C/T]TCTTGTGGCCTTTTC | 79058 |
rs187968992 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010152 | GTCTCGAACTCCTGA[C/T]CTCAGGTGATCTGCC | 79058 |
rs188241201 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989157 | AGGTTGCAGTGAGCC[A/G]ACATCACACCACTGC | 79058 |
rs188275204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995056 | GAGCCCGGGCTGCCC[C/T]GAAACCTCCCTCGGC | 79058 |
rs188498407 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999711 | TGTCCCCTGGGCACT[C/T]GTGCTACGTGTCCCG | 79058 |
rs188512761 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981167 | AGAGAAGGGCCTGGC[A/G]GGAGGTTGGCTGATG | 79058 |
rs188516129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81980651 | TAGCCTCCAGCCAGA[A/G]GCTGGAAACAGACAC | 79058 |
rs188743828 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007951 | GCCCCACTGCCGAGC[C/T]GTGGTCAGCCCTCAC | 79058 |
rs188761797 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987848 | GCAAAACTCCATCTC[A/C]AAAAAACAAAAAAAC | 79058 |
rs188774557 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003020 | GCTGGGATTACAGGT[G/T]CCCGTTTAGTAGAGA | 79058 |
rs188780858 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989515 | TTCTTCTTTCATGTG[A/T]TTCGGAGGAGGTCTG | 79058 |
rs188805505 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81998807 | GTTCTGGAAGTTCTC[C/T]GAAGGTTATGGCCAC | 79058 |
rs189045478 | snp | C/T | 9.39311e-05 | 0.0068525 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81983642 | ATGGTGCCCGCTTCC[C/T]GGAGCCGTGAGGGGC | 79058 |
rs189140525 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010535 | CTCCATCTCAAAAAA[A/G]AAAAAAAAAAAAAAA | 79058 |
rs189162027 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995342 | ATTCCCCGCATTTAT[A/C]CCCATTTGGAAGCTC | 79058 |
rs189172969 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011077 | CTTGCTCCAGGTGCC[C/T]GGCCCCAGCTCAGGG | 79058 |
rs189175836 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976374 | GGTTCTGAGGTTGCA[C/G]AGAGCATGGGACTGG | 79058 |
rs189206105 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990505 | AGTTTGGGATCTTCC[A/T]CGCCGAGCTCTGGGG | 79058 |
rs189288473 | snp | A/G | 3.58686e-05 | 0.00423474 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82017054 | CTGAGCCCATCCCAG[A/G]GACGGCCCAGCCCGT | 79058 |
rs189395402 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992364 | CCCTCCCTGAGATCC[C/T]GCATGAGGGAGGGAA | 79058 |
rs189405220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000249 | CTGCAGAGCGTGGGG[C/T]GTGGAGCATGGGGCT | 79058 |
rs189420247 | snp | G/T | 0.00150883 | 0.0274251 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011649 | GCCTCCAGTGCTCGG[G/T]GCCTTGGTGCTGTGG | 79058 |
rs189675387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994044 | GGGAGTTGGAAACGC[A/G]GAGGCAAGCCCGCCT | 79058 |
rs189692845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991977 | AAAGAATATGCCCTC[A/G]AAGCCAGCAGCAGAG | 79058 |
rs189941405 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016343 | GGAAGCTGGGCGATG[C/G]GCTCATGGGGGCCGG | 79058 |
rs190009067 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997920 | TAACCTCCACCTCCC[C/G]GGTTCAAGCGATTCT | 79058 |
rs190025024 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978610 | ACGACTCGGAGTTTG[C/T]GGGAGCAGCCCACGG | 79058 |
rs190062453 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001730 | GTTGGGCCCAAGATC[A/C]CCTGGTTGGGATTGT | 79058 |
rs190088201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | ASPSCR1 | GRCh38.p7 | 17:81982616 | TTAATTCTTCCAGAT[A/G]CCCCTGGGCTGTCTG | 79058 |
rs190225990 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006753 | CCCTCACAGTGTCTC[A/G]TCCCTCAACCTCTGT | 79058 |
rs190348988 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000970 | AGGCTGGGTCTGCCC[A/G]CACGGGCTGGCGGCT | 79058 |
rs190441289 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010073 | CGCTACCACTAGCTC[A/G]GCTAATTTTTGTTGT | 79058 |
rs190449204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988783 | TTGCGGGGCATCTGG[C/T]TGTGTCTCAGGGCAT | 79058 |
rs190592233 | snp | A/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986153 | CACAGTGGCTGGGCA[A/C]AGTGGCTGGGCAAAG | 79058 |
rs190673778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992575 | CTCATGACCATCTCC[A/G]GACCCCTGGCCATCT | 79058 |
rs190686546 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012877 | CTGGGCCGCCCTCCA[A/G]AGCCAGAAGCAATGA | 79058 |
rs190706162 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012415 | AAGCCTTTGAGAGCC[A/G]GTGGGTTCCGAGGGG | 79058 |
rs190729286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002350 | TGCAACCTTCCCCTC[C/T]CAGTTCAAGTAATTT | 79058 |
rs190734493 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982141 | GCCTGGCTAATTTTT[A/G]TATTTTTAGTAGAGA | 79058 |
rs190970193 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988422 | ATTGCGCCACTGCAC[G/T]CCAGCCTGGGTGACA | 79058 |
rs191065718 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014640 | TCTTGAGCTGCAAGG[G/T]CTCCTCTCTTGGCTT | 79058 |
rs191242866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996965 | GCAGAGGAACCCAAA[C/T]GCGCAGAGGAACCCA | 79058 |
rs191307933 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999945 | ACTGTTCCTGTTGAG[C/T]GGACAAGGGAGTGGG | 79058 |
rs191326587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981352 | CAGTTGGTTGGGGGG[A/G]GCTTAGGGTTTCATT | 79058 |
rs191333325 | snp | C/T | 0.000610008 | 0.0174537 | missense, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015298 | CACCATCCCCTCGTC[C/T]GAGCAGTGGCGATCC | 79058 |
rs191365132 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993359 | GCTGGGACCACAGGC[A/G]CCCGCCACCACGCCT | 79058 |
rs191472057 | snp | C/G | 0.00716266 | 0.059414 | upstream-variant-2KB, intron-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977170 | CCGTACAGGGGCGGG[C/G]GGACTGCCCCAAACC | 79058 |
rs191558406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005164 | GGTGCCGAGTGTTCC[A/G]GAAATATTGCTGGTT | 79058 |
rs191576563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984643 | GAGGGTCAGGAATCT[A/G]GGAGCAGCTTAGCTC | 79058 |
rs191808455 | snp | A/G | 6.20367e-05 | 0.00556906 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009534 | GGCCTTCAGGGAGGC[A/G]CAGATAAAGGAGAAG | 79058 |
rs192034171 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003600 | GGGATTCGAGGCCTG[A/G]TGCCTCTGCCTGGTG | 79058 |
rs192105222 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988633 | TCATTTGATGAACAC[A/T]CACACCTGTGGTGGA | 79058 |
rs192134974 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011078 | TTGCTCCAGGTGCCC[A/G]GCCCCAGCTCAGGGA | 79058 |
rs192198359 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993986 | CTGCAAGGAAGGCCT[G/T]AGAAGGGCTTTTGTT | 79058 |
rs192205332 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015562 | TCTCTGCATCGGTGG[C/T]CTCTGAGGGAGCCCT | 79058 |
rs192233112 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005769 | CCAGACCACGGCGGA[C/T]GGAGGCGTCCTGCTG | 79058 |
rs192357932 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983279 | CTGGGGCTGTCAGCA[C/G]CCCAGACTCTGAAGG | 79058 |
rs192423465 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989936 | GGGATTACTGGCGCA[C/T]GCCATCACGCCTGGC | 79058 |
rs192474592 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989292 | ACCATGGAGCAGGAT[A/G]TGGACGAGGTTTCAT | 79058 |
rs192589467 | snp | A/G/T | 0.0029348 | 0.0382022 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82016494 | AACCTCTTCCCGGCC[A/G/T]CTCTGGTGCACTTGG | 79058 |
rs192633842 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985970 | GATGGGATCATAAGG[C/T]CTCTTTTTTTTAAGA | 79058 |
rs192734516 | snp | A/G | 0.030278 | 0.119257 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010169 | TCAGGTGATCTGCCC[A/G]CCTCGGCCTCCCAAA | 79058 |
rs192848784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994543 | TCCACGTCCTGCCAG[C/T]GGCCCCGAGACTGGA | 79058 |
rs192865562 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81998958 | CCCTCACGCCTCCCC[C/G/T]CAACCGTGGGGACCT | 79058 |
rs193007456 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81980028 | ACTCTTGTCGCCCAG[A/G]CTGGAGTGCAGTGGC | 79058 |
rs193066150 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81980807 | CCTGCCTCTTCACGG[C/G]TCCTATGTGCAAAAA | 79058 |
rs193227178 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81998425 | TTTTCTTCCTGTGTT[A/G]CAGCGAATGGGCCTC | 79058 |
rs199630997 | snp | A/G | 1.66391e-05 | 0.00288431 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82011545 | TTCTCCTCTGCAGTG[A/G]GGGACTTGCGAGACT | 79058 |
rs199635423 | snp | C/G | 0.000134095 | 0.00818717 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011519 | GTGGAAGAGCTGTCT[C/G]TATGTTCTTTTTCTC | 79058 |
rs199665633 | snp | A/T | 0.00867336 | 0.0652798 | splice-acceptor-variant, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015073 | CCACTTTCCCTTTCC[A/T]GCCCCAGCTTGGTGA | 79058 |
rs199668336 | snp | A/G | 3.32436e-05 | 0.00407685 | intron-variant, synonymous-codon | ASPSCR1 | GRCh38.p7 | 17:82012214 | CTTCCTAACACGTAG[A/G]TGCCTTCTCTCCTCA | 79058 |
rs199809269 | snp | A/T | 0.00141582 | 0.0265689 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81996388 | GGGGTAGGCACCACA[A/T]GGTGCTTCCCTTGTC | 79058 |
rs199934562 | snp | C/T | 1.70731e-05 | 0.00292169 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996596 | CCTGCTGCGAGCACA[C/T]TCAGGAGAAGCAGAG | 79058 |
rs199964378 | snp | C/T | 3.78415e-05 | 0.00434964 | intron-variant, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996890 | GGGGGTGTCCTTTCT[C/T]CTGATGTGTAGCCCT | 79058 |
rs200015531 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001996 | TTTTCTTTTTTTTTT[C/T]TTTTTCCTTTTTTTT | 79058 |
rs200052112 | snp | C/G/T | 0.000150437 | 0.00867175 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81996371 | CGGGAGAGGGTGAGC[C/G/T]GGGGGTAGGCACCAC | 79058 |
rs200185405 | in-del | -/G | 0.0209421 | 0.100162 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81979975 | GTCCTGTTTTCTGGT[-/G]TTTTTTTTGTTTTGT | 79058 |
rs200395026 | in-del | -/TG | | | intron-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009594 | GGATGTGGGGGCGAC[-/TG]AGGCACAGCTCTGAG | 79058 |
rs200437145 | snp | A/G | 8.32563e-05 | 0.00645145 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82010835 | TTCCCCGACCGCTAC[A/G]TCCTACAGGGCTTCT | 79058 |
rs200441382 | snp | A/G | 0.00100494 | 0.0223933 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016906 | GGCACCTCCCGTGGC[A/G]GCACTCACCACTCTG | 79058 |
rs200558937 | snp | A/G | 7.16268e-05 | 0.005984 | missense, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015154 | CAGAGCAGAGAACAC[A/G]CTTGCCAGTGGTAGG | 79058 |
rs200573155 | snp | C/T | 0.000151071 | 0.00868981 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82017272 | CGGGTGGTGAGAGCC[C/T]GGGGTGTGTGGTCAC | 79058 |
rs200591341 | snp | C/T | 0.000117959 | 0.00767892 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011500 | GCAGCCCGGGGCTGG[C/T]GTGGTGGAAGAGCTG | 79058 |
rs200628867 | in-del | -/TG | 0.00755907 | 0.0610114 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984985 | ACACACCCACACACC[-/TG]CGTGCACACCCCCCC | 79058 |
rs200650232 | snp | C/G/T | 0.00235783 | 0.0342556 | intron-variant, missense, stop-gained | ASPSCR1 | GRCh38.p7 | 17:82012185 | GGGCGCATGGATGGG[C/G/T]GAGGTCCACGGTGCT | 79058 |
rs200674638 | snp | C/T | 0.000240414 | 0.0109612 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996466 | AAGACCCCAGGAAGC[C/T]TGGGCTCGTCAGCGT | 79058 |
rs200690070 | snp | G/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007896 | GATGGTTGTGGCTTT[G/T]GAAGGGCAGCCCCCA | 79058 |
rs200701013 | snp | A/C/G | 0.00968055 | 0.0690223 | utr-variant-3-prime, nc-transcript-variant, synonymous-codon | ASPSCR1 | GRCh38.p7 | 17:82017350 | TGAGGTGCCCACTCC[A/C/G]CCAGCCACAGGACCA | 79058 |
rs200865502 | snp | A/G | 0.000513731 | 0.0160188 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009150 | CTTTGAGCTGACGGT[A/G]GACGACGTGAGAAGA | 79058 |
rs200910990 | in-del | -/TCTTT | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982791 | CTTTTTCTTCCTTTC[-/TCTTT]TCTTTTCTTTTCTTT | 79058 |
rs200933354 | in-del | -/G | 0.0221141 | 0.102801 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997326 | ATTCAGAAATCTCTA[-/G]AAAAGGGGTGGTAAC | 79058 |
rs200941868 | snp | C/T | 0.00196759 | 0.0313038 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996808 | GAGCAGGAGCAGGAG[C/T]GGGAGCGGGATCCCC | 79058 |
rs200964753 | snp | A/C/G/T | 0.000418072 | 0.0144532 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016879 | GGCCAGGTAAGTGCC[A/C/G/T]GTGGGTCTGGGGGCA | 79058 |
rs201013408 | snp | A/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81998675 | TTATTTTATTGGCTT[A/C]TGCATGTGTGTTCAT | 79058 |
rs201030136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016470 | AGCCCCCCGCCCTCC[C/T]TGCAGGCGAACCTCT | 79058 |
rs201080102 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990044 | CCTCCCAAAGTGCTG[A/G]GATTACAGGCGTGAG | 79058 |
rs201134448 | snp | C/T | 7.45143e-05 | 0.00610341 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82017067 | AGGGACGGCCCAGCC[C/T]GTGAAGAGGAGCCTG | 79058 |
rs201221183 | snp | A/G | 0.00150941 | 0.0274304 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011647 | CTGCCTCCAGTGCTC[A/G]GGGCCTTGGTGCTGT | 79058 |
rs201251995 | in-del | -/TTTTCTTTCT | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982718 | CAGATTTTTCTTTTC[-/TTTTCTTTCT]TTTTCTTTCTTGTTT | 79058 |
rs201260656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988530 | GGAGGTGGTGGGGCC[A/G]TTGGTGGTAAAGCCC | 79058 |
rs201260961 | snp | C/T | 0.000101015 | 0.00710615 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985473 | ATAGTTGCTTTTCTT[C/T]CTAAGGAAGTTTCTC | 79058 |
rs201353658 | in-del | -/TTTC | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982804 | TCTCTTTTCTTTTCT[-/TTTC]TTTCCTTTCCTTTCC | 79058 |
rs201380867 | snp | C/T | 3.39455e-05 | 0.00411966 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996624 | GAGCACAAGGGCACC[C/T]GCAGCTGCCCCCTTT | 79058 |
rs201439503 | snp | A/G | 0.00070542 | 0.0187673 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010878 | AGACAGGTGGGCAGC[A/G]CTGTGGGGTGTCCGG | 79058 |
rs201473706 | snp | A/G | 3.48365e-05 | 0.00417337 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996483 | GGGCTCGTCAGCGTC[A/G]GCTGGCCAGGCAGCC | 79058 |
rs201508476 | snp | A/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010541 | CTCAAAAAAAAAAAA[A/C]AAAAAAAAAAACCAG | 79058 |
rs201515044 | snp | C/T | 0.000455029 | 0.0150767 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81996415 | TGTCCTCTGGCCCCA[C/T]TCAGGTTTGTCATGA | 79058 |
rs201544231 | snp | C/T | 3.34264e-05 | 0.00408804 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82010861 | CTTCTTCCGCCCCAG[C/T]GAGACAGGTGGGCAG | 79058 |
rs201587826 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012300 | TACCTGAGGGCCTCC[A/C]TGGGGTGCTGCGGGG | 79058 |
rs201590427 | in-del | -/T | | | upstream-variant-2KB, downstream-variant-500B | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81975623 | GGCTAATTTTTGTAC[-/T]TTTTTTTTTAAGTAG | 79058 |
rs201700837 | in-del | -/G | 0.235854 | 0.249599 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997484 | GATTTTTTTTTTTCT[-/G]GGGTTTTTTTTTTTT | 79058 |
rs201729186 | snp | C/T | 0.00199794 | 0.0315432 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012311 | CTCCCTGGGGTGCTG[C/T]GGGGCGGGGCCCTCC | 79058 |
rs201736615 | in-del | -/C | 0.0372196 | 0.131242 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009914 | TGATTTAGAATGAAA[-/C]CTTTTTTTTTTTTTG | 79058 |
rs201786107 | snp | C/G/T | 3.38129e-05 | 0.00411161 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996643 | GCTGCCCCCTTTGTT[C/G/T]CTTTCTCGGGTGGGG | 79058 |
rs201931527 | snp | C/T | 7.25571e-05 | 0.00602273 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82017057 | AGCCCATCCCAGGGA[C/T]GGCCCAGCCCGTGAA | 79058 |
rs202008716 | snp | C/G | 0.000149582 | 0.0086469 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82012281 | ACGCAGACCCTCTTT[C/G]AGGTACCTGAGGGCC | 79058 |
rs202046657 | in-del | -/CCA | 0.0460142 | 0.144533 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985048 | GCACACACCTCCCCC[-/CCA]CACACACCCACGCAC | 79058 |
rs202058036 | in-del | -/CCCACACCCG | 0.0150606 | 0.0854603 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984930 | CAACGTGCACACACC[-/CCCACACCCG]CACACACCCGCACAC | 79058 |
rs202095235 | snp | C/T | 4.03397e-05 | 0.0044909 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81983566 | CAGGTTTCAGAGGAG[C/T]GTGCTCGACCTTTCT | 79058 |
rs202149445 | snp | A/C/G | 0.000964633 | 0.0219408 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82010826 | AGGGTCCTGTTCCCC[A/C/G]ACCGCTACGTCCTAC | 79058 |
rs202177519 | snp | C/T | 0.00598996 | 0.0543976 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009000 | GCGGAGGGCCCAGCC[C/T]GTGACACCCGCCGTC | 79058 |
rs202236624 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009814 | CTGTGGATGGGACGT[A/G]GGGGCGACTGAGGCA | 79058 |
rs367621864 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81998050 | CAGGCTGGTCTCGAA[C/T]TCCTGACCTCAGGTG | 79058 |
rs367640413 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987749 | GCTGGCTTTGGTGGT[A/G]GCTGTGGGGGTGGGT | 79058 |
rs367665050 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015465 | GTGTTCCCGAGTCCT[A/G]CCCGCCCCTTTCTGT | 79058 |
rs367721710 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011809 | GCCAGGCGGTGGGAG[C/T]CAGGCTTCCTGCCTT | 79058 |
rs367747020 | snp | A/C/T | 0.000206578 | 0.0101611 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996566 | GCCGTCCGGAGGACG[A/C/T]GGACACCTCAGGGCC | 79058 |
rs367750451 | snp | C/T | 0.000153988 | 0.00877328 | utr-variant-3-prime, nc-transcript-variant, missense | ASPSCR1 | GRCh38.p7 | 17:82017346 | AGCCTGAGGTGCCCA[C/T]TCCGCCAGCCACAGG | 79058 |
rs367763122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984509 | GTGAACCCGGGAGGC[A/G]GAGCTTGCAGTGAGC | 79058 |
rs367770038 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001012 | TGCCCCTCCCGCCTC[A/G]GGGGTGAACCTTGCT | 79058 |
rs367845443 | in-del | -/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002891 | ATAACTTTTTTTTTT[-/T]CGAGACAGGGTCTGT | 79058 |
rs367883577 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996967 | AGAGGAACCCAAACG[C/T]GCAGAGGAACCCAAA | 79058 |
rs367961644 | snp | A/C | 0.00319074 | 0.0398324 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008711 | TCGCCACCCCTCCCC[A/C]CCATGGAGACCCTGA | 79058 |
rs368050708 | snp | G/T | 1.73213e-05 | 0.00294284 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82017031 | TGAGGAGGGGGCGCT[G/T]GTCCCCCCTGAGCCC | 79058 |
rs368102468 | in-del | -/TGCC | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013496 | GCCTGCCTGCCTGCC[-/TGCC]GTCAGAGAGCTGGCG | 79058 |
rs368133960 | snp | A/C | | | intron-variant, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996947 | GGCGTGGCCGTGATG[A/C]GGGCAGAGGAACCCA | 79058 |
rs368135166 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978340 | ATCCTGGCTAAAACG[A/G]TGAAACCCCGTCTGT | 79058 |
rs368141370 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989938 | GATTACTGGCGCACG[C/G]CATCACGCCTGGCTA | 79058 |
rs368146790 | snp | A/C/G | 7.06706e-05 | 0.00594399 | missense, utr-variant-5-prime, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81983601 | AGTGGAGATTTGCCA[A/C/G]CCTGCCCAACAATGC | 79058 |
rs368164103 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015018 | TGCCTCCCTCAAAGG[C/T]CCTTCCCGGGCCCTG | 79058 |
rs368168243 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012021 | GGCTGCACGGGTGGT[A/G]TCCCCTGCAGGTGGG | 79058 |
rs368174362 | snp | A/G | 4.98708e-05 | 0.00499328 | intron-variant, missense | ASPSCR1 | GRCh38.p7 | 17:82012213 | GCTTCCTAACACGTA[A/G]GTGCCTTCTCTCCTC | 79058 |
rs368179927 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008306 | TCCCCAGGTGTCGAG[A/C]GTGTGAGGTAGGAGT | 79058 |
rs368182474 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004704 | AGTGCAGTGCCGGCT[C/G]CTGGACCCTGCTGTG | 79058 |
rs368221513 | snp | G/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993503 | CAGGCGTGAGCCACC[G/T]CGCCCGGCTGAGTCC | 79058 |
rs368228148 | snp | A/G | 0.000528989 | 0.0162547 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994911 | GCTCACCCAGTCCCC[A/G]CTCACTTTCAGCCCA | 79058 |
rs368230520 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984887 | CCGCACACACACCCC[C/G]CACACACACCCACAC | 79058 |
rs368306368 | snp | C/T | 2.16186e-05 | 0.00328768 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81983665 | TGAGGGGCCTGAGAA[C/T]ATGGTGGGTCGTGCT | 79058 |
rs368324606 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978573 | CTGCTGCGTGGGGGA[C/T]CGTGAGGATCCGAAG | 79058 |
rs368331509 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008470 | CATTGAAATCACTGC[C/G]CAGGGCTCCGCGAGC | 79058 |
rs368335095 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989348 | GTGAGGGTGGAGTGC[C/T]TGGTGGGCTCTCTGC | 79058 |
rs368337244 | in-del | -/TTTCCAC | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014229 | GTCCTTCCTTTCCAC[-/TTTCCAC]CCAGGACAGCCCCGT | 79058 |
rs368349085 | snp | A/G | 0.000133182 | 0.00815926 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015385 | CTCAGTGCTCCCTGC[A/G]CAGAGGCGCAGACAG | 79058 |
rs368381332 | snp | C/T | 0.000117348 | 0.00765901 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011646 | CCTGCCTCCAGTGCT[C/T]GGGGCCTTGGTGCTG | 79058 |
rs368561373 | snp | C/G/T | 0.000419044 | 0.0144699 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996013 | GGTGAAGCTGCCCTG[C/G/T]GGGGCACGACGCTGC | 79058 |
rs368626744 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992860 | GCGCAGAGGACACCC[A/G]CCGTGTGTGTGGTGC | 79058 |
rs368658956 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013819 | GTGGGGAACAAAGCC[C/T]CCCGCCCCTGCCTGA | 79058 |
rs368684378 | snp | G/T | 1.69513e-05 | 0.00291125 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996765 | CTCCAAGCCAAAGAA[G/T]TCCAAGTCGGGCCAG | 79058 |
rs368689439 | snp | A/G | 0.433963 | 0.169285 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009743 | CCCCCTGTGAGGTCT[A/G]TGGATGGGACGTGGG | 79058 |
rs368707985 | in-del | -/TGGGACGGGGATGGCGGGGCGTGGATGG | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983473 | GCGGGGCGTGGATGG[-/TGGGACGGGGATGGCGGGGCGTGGATGG]CAGGGCGTGTCAGGC | 79058 |
rs368728773 | snp | A/G | | | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82016515 | GTGCACTTGGGAGCC[A/G]AGGAGCCGGCAGGTG | 79058 |
rs368765562 | snp | C/T | 1.67584e-05 | 0.00289464 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016912 | TCCCGTGGCGGCACT[C/T]ACCACTCTGTGTCTT | 79058 |
rs368821082 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001583 | TTTGGTGAGGAACCC[C/T]GGGGGGTAGGGGGTG | 79058 |
rs368891300 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999724 | CTCGTGCTACGTGTC[C/T]CGGAACTCAGGTGAG | 79058 |
rs368905634 | snp | C/T | 0.00027973 | 0.0118231 | intron-variant, missense | ASPSCR1 | GRCh38.p7 | 17:82012173 | CTGTCTTCCTTCGGG[C/T]GCATGGATGGGCGAG | 79058 |
rs368938644 | snp | C/T | 0.000166143 | 0.00911285 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985499 | TTCTCATGTCTTATA[C/T]CCTCCAGGTTCGCAT | 79058 |
rs368954140 | snp | A/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984793 | CACACCCACACACAC[A/C]CCCACACACCCACAT | 79058 |
rs368957042 | snp | A/G | 0.000189824 | 0.00974042 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996544 | GAGCTCAGCCGCGGC[A/G]ACTTGAGCCGTCCGG | 79058 |
rs369017225 | in-del | -/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985043 | CACACACCTCCCCCC[-/C]ACACACACCCACGCA | 79058 |
rs369076013 | snp | C/T | 1.89109e-05 | 0.00307491 | intron-variant, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996888 | TTGGGGGTGTCCTTT[C/T]TCCTGATGTGTAGCC | 79058 |
rs369083342 | snp | C/T | 4.97583e-05 | 0.00498765 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81985515 | CCTCCAGGTTCGCAT[C/T]GCTTTGCAGCTGGAC | 79058 |
rs369139907 | snp | A/G | 4.3083e-05 | 0.00464108 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996024 | CCTGCGGGGCACGAC[A/G]CTGCAGTCGCTGGGC | 79058 |
rs369202822 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81996375 | AGAGGGTGAGCCGGG[G/T]GTAGGCACCACAAGG | 79058 |
rs369336875 | in-del | -/C | 0.0975279 | 0.198122 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985001 | ACACCTGCGTGCACA[-/C]CCCCCCACACACCTG | 79058 |
rs369384915 | in-del | -/CT | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002003 | TTTTTTTTCTTTTTC[-/CT]TTTTTTTTTTTTTTT | 79058 |
rs369392943 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, missense | ASPSCR1 | GRCh38.p7 | 17:82017396 | GGAATAAAGACTTGT[A/G]CATCCCTCAACGCCT | 79058 |
rs369415476 | snp | C/G/T | 1.70504e-05 | 0.00291975 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994888 | GATGAGGTAGGCGGC[C/G/T]TGCTCTTGCTCACCC | 79058 |
rs369447543 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984979 | ACCTGCACACACCCA[C/G]ACACCTGCGTGCACA | 79058 |
rs369490795 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013648 | AGGGGCCGGCCCCCG[A/G]CTTCCGAGAGGGACA | 79058 |
rs369503779 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009630 | CCCCCCGTGAGGTCT[A/G]TGGACGGGATGGGGC | 79058 |
rs369543467 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009809 | GAGGTCTGTGGATGG[C/G]ACGTGGGGGCGACTG | 79058 |
rs369595227 | snp | A/G | 0.000185374 | 0.00962562 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985620 | CAGGTGAGCATCAGT[A/G]GGCTGGGGGCTCTTC | 79058 |
rs369768144 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990898 | GGGATACTGTAGCAC[A/G]TCTGGGCAGTCCACG | 79058 |
rs369771511 | snp | A/G | 0.000486263 | 0.0155851 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009013 | CCCGTGACACCCGCC[A/G]TCAGCCGCGCCCTCT | 79058 |
rs369804118 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005480 | GGCTCTCAGCCACCC[C/T]GTTGGCTGAGTGAGA | 79058 |
rs369820176 | snp | G/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014671 | CGTTCCCCGGAGGGT[G/T]GTGCTGTTCTCGTTG | 79058 |
rs369843263 | snp | C/T | 0.000424358 | 0.0145602 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82016493 | GAACCTCTTCCCGGC[C/T]GCTCTGGTGCACTTG | 79058 |
rs369882046 | snp | A/G | 0.000103607 | 0.00719673 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983714 | GTGGGGCACAGGATC[A/G]TTCAGCTGGCCAGGG | 79058 |
rs369912147 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002507 | TGATCCACTTGCATC[A/G]GCCTCCCAAAGTGCT | 79058 |
rs369914067 | snp | A/G/T | 3.23965e-05 | 0.00402458 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82009123 | CTGGCCAGCGGAGCT[A/G/T]CCTGATGAGTTCTTT | 79058 |
rs369975443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005770 | CAGACCACGGCGGAC[A/G]GAGGCGTCCTGCTGA | 79058 |
rs369989145 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994676 | GCTGAGGTCTGTGGC[C/G]TGGGCCTGGGCCTGG | 79058 |
rs370033875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997899 | TGGCGCACTTTCGGC[C/T]CACTGTAACCTCCAC | 79058 |
rs370077758 | in-del | -/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009723 | GAGGCACAGCTCTGA[-/G]CGGGCCCCCTGTGAG | 79058 |
rs370150951 | snp | A/G/T | 0.000232593 | 0.0107818 | missense, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015180 | GTAGGAGATGGAGGC[A/G/T]ACGTGGACTCTGGGA | 79058 |
rs370178683 | snp | C/T | 8.33493e-05 | 0.00645505 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81994839 | GTGCCTGCAGCACCC[C/T]GGCGGGGCCACCCCA | 79058 |
rs370225186 | snp | C/T | 0.000311951 | 0.0124851 | intron-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009459 | CATTCTGACCAGAAG[C/T]CCTGTTCCTTCCCCT | 79058 |
rs370250013 | snp | A/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001891 | TTTATCCACAGTGAC[A/C]CACGCCTGCCACACC | 79058 |
rs370380394 | snp | C/T | 8.34369e-05 | 0.00645844 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011534 | GTATGTTCTTTTTCT[C/T]CTCTGCAGTGGGGGA | 79058 |
rs370459829 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983860 | GAAAATGAGCATCTC[A/G]TGTTTTTTTTTTTTT | 79058 |
rs370497131 | snp | A/G | 2.897e-05 | 0.0038058 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983530 | CTCTGCAGGGCAGCA[A/G]GTGTGCTCTGGTCTG | 79058 |
rs370514086 | snp | A/G | 1.65954e-05 | 0.00288053 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82011587 | CACCTGGGGAACCCC[A/G]AGCTGTCATTTTACC | 79058 |
rs370519323 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005815 | GGATGTGGGAAGGGG[C/T]GGAGGCACAGCTCCA | 79058 |
rs370541724 | in-del | -/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993585 | CAGTGGACCCCTGCG[-/G]CCCTGTAAGCACACA | 79058 |
rs370550502 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981883 | GTGGACCAGGCTGGT[C/G]TCAAACTCCTGACCT | 79058 |
rs370646730 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81996287 | ATCTTGGGAGGGCGC[A/G]TGGGGCAGGAGAGGG | 79058 |
rs370670538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006167 | GTCCTTGTGGGTGCA[C/T]GTGTGTGCACGGGTG | 79058 |
rs370719752 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986389 | AGCCGAGATCGCACT[A/G]CTGCACTCCAGCCTG | 79058 |
rs370721353 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003965 | GGAGCCCTGGCGGGG[C/T]AGGCCGGGCCGAGAC | 79058 |
rs370768612 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001113 | GTGGGACTCGTGGGG[C/T]GGGGAGGAGCCTGTC | 79058 |
rs370883621 | snp | A/G | 0.000100844 | 0.00710012 | utr-variant-3-prime, nc-transcript-variant, missense | ASPSCR1 | GRCh38.p7 | 17:82017325 | CAGCAAGAGGTGAGA[A/G]CTGCCAGCCTGAGGT | 79058 |
rs370909339 | snp | C/T | 1.64819e-05 | 0.00287066 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81979165 | TCAGCAGTTCACCAT[C/T]CTTTCATCTCACCCC | 79058 |
rs370921904 | in-del | -/CC | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002002 | TTTTTTTTTCTTTTT[-/CC]TTTTTTTTTTTTTTT | 79058 |
rs371044315 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983515 | GCAGGGCGTGTCAGG[C/T]TCTGCAGGGCAGCAA | 79058 |
rs371051697 | snp | C/T | 0.000259977 | 0.0113983 | missense, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015090 | CCCCAGCTTGGTGAC[C/T]GGGTGGCTCCATTCA | 79058 |
rs371078443 | snp | A/G | 0.000159987 | 0.00894248 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82017150 | TGGGGTGCTGTGGCC[A/G]GGTGGAGGGCGGGGG | 79058 |
rs371107357 | snp | A/G | | | upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977424 | GGCGAGCCCATCCAA[A/G]CCGCGCTTCCCGGAG | 79058 |
rs371225128 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993289 | CGCGATCTCGGCTCA[C/T]TGCAAGCTCCACCTC | 79058 |
rs371281656 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004310 | GTCCTTAGTCCTGCC[C/T]GTCCTTTCTGGCCTT | 79058 |
rs371380745 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008368 | ACTCCCGACAGCTCT[C/T]GGCTGTTCTGTGTGA | 79058 |
rs371423253 | snp | C/G/T | 4.99325e-05 | 0.00499641 | intron-variant, missense, synonymous-codon | ASPSCR1 | GRCh38.p7 | 17:82012203 | GGTCCACGGTGCTTC[C/G/T]TAACACGTAGGTGCC | 79058 |
rs371452816 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000456 | GCGCCTCCCATCGCC[A/G]CCAGCCGCACACGCA | 79058 |
rs371480308 | snp | C/T | | | utr-variant-3-prime | ASPSCR1 | GRCh38.p7 | 17:82018044 | CCTGGGGCCTGACTC[C/T]CTACCCTTTCCCCTC | 79058 |
rs371480391 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014273 | GTCGCCCACTGCCGG[A/G]GCCTCTCTGGGACCA | 79058 |
rs371491882 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993252 | GGAGTCTCGCTCTGT[C/T]GCCCAGGCTGGAGTG | 79058 |
rs371509892 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995748 | TTGGGTCCCAGCTGC[A/G]GAGACCAGGCTGGGG | 79058 |
rs371537189 | snp | A/C/G | 0.000100534 | 0.00708927 | synonymous-codon, missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996693 | TCCTGGGCCCACGAG[A/C/G]CCTCTGACATCATCT | 79058 |
rs371596988 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978574 | TGCTGCGTGGGGGAC[C/T]GTGAGGATCCGAAGG | 79058 |
rs371621642 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996985 | AGAGGAACCCAAACG[C/T]GGGGCTCTGGACAGG | 79058 |
rs371657939 | snp | A/G | 0.000228012 | 0.0106749 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996815 | AGCAGGAGCGGGAGC[A/G]GGATCCCCAGCAGGA | 79058 |
rs371709768 | snp | G/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984526 | AGCTTGCAGTGAGCC[G/T]AGATTGTGCTGCCAC | 79058 |
rs371810029 | snp | A/C | 2.79748e-05 | 0.00373987 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995944 | GGGCTTCCCTGGGCT[A/C]TGGGGTCCCGGTGCA | 79058 |
rs371864329 | in-del | -/TCTT | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982764 | CTTTCTTTCTTTCTT[-/TCTT]CTTCTCTTTTTCTTT | 79058 |
rs371875028 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988853 | TTGCACCTGGTCACC[C/T]ACCCCAGCTTCTCCT | 79058 |
rs371903775 | snp | C/T | 1.66098e-05 | 0.00288177 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985501 | CTCATGTCTTATACC[C/T]TCCAGGTTCGCATCG | 79058 |
rs371915284 | snp | A/G | 0.000169963 | 0.00921697 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82017161 | GGCCGGGTGGAGGGC[A/G]GGGGTCCGGGTGCTG | 79058 |
rs371971833 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995663 | CTGCCTCTCTCGCTC[C/T]GGGCAGTGGGTCCTG | 79058 |
rs372038468 | snp | C/T | 0.000401526 | 0.0141634 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016462 | GGCCCCTGAGCCCCC[C/T]GCCCTCCCTGCAGGC | 79058 |
rs372049622 | in-del | -/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010265 | CCGGGCGTGGTGGCT[-/C]ACGCCTGTAATCCCA | 79058 |
rs372050513 | in-del | -/T | 0.649163 | 0.19032 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010087 | GGCTAATTTTTGTTG[-/T]TTTTTTTTTTTTTTA | 79058 |
rs372073944 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989486 | GCAGAGTGGGACGGG[C/T]GGGAAGCTGATGTTT | 79058 |
rs372090904 | snp | A/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009846 | AGCTCTGAGCAGGGC[A/C]CCCCCGTGGTGGCGC | 79058 |
rs372104369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997984 | GGCGTGTGCCACCAC[A/G]CCCAGCTAATTTTTG | 79058 |
rs372109918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985323 | TGGTGCAGCCCTGCC[A/G]GGGAGCCTCCAAGGC | 79058 |
rs372128517 | snp | G/T | 0.000472311 | 0.0153601 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996654 | TGTTCCTTTCTCGGG[G/T]GGGGGACAGAGACTG | 79058 |
rs372171143 | snp | A/C/T | 0.0123036 | 0.0774623 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985048 | GCACACACCTCCCCC[A/C/T]CACACACACCCACGC | 79058 |
rs372177769 | snp | A/G | 9.34256e-05 | 0.00683404 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82017068 | GGGACGGCCCAGCCC[A/G]TGAAGAGGAGCCTGG | 79058 |
rs372210210 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011393 | TGGCCCAGCCACGCC[G/T]AGCACCTGGAGTGCT | 79058 |
rs372226554 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999924 | TGTCCCCCTGGCTGT[C/T]CTGGGACTGTTCCTG | 79058 |
rs372283666 | in-del | -/CGTGGACCGGGAGCC | | | cds-indel, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82009054 | CGTGGACCGGGAGCC[-/CGTGGACCGGGAGCC]GGTGGTGTGCCACCC | 79058 |
rs372300609 | snp | C/T | 3.44762e-05 | 0.00415174 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996553 | CGCGGCGACTTGAGC[C/T]GTCCGGAGGACGCGG | 79058 |
rs372341903 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014403 | GCAGCCCCCACTCCC[A/G]CTCTGTGGGTGGATG | 79058 |
rs372360008 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81998176 | AGGTCTCTCTCTGTT[G/T]CCCAGGCTGGTCTCG | 79058 |
rs372380480 | snp | C/T | 1.76176e-05 | 0.00296791 | missense, utr-variant-5-prime, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81983616 | ACCTGCCCAACAATG[C/T]CAAGCTGGAGATGGT | 79058 |
rs372470623 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000510 | TGCTGGGTCCCTTTC[A/G]GTGATGGGGGGAGGG | 79058 |
rs372486537 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004525 | CTTTCACAGCTGCCC[A/G]GCCACCCTCGGAGCC | 79058 |
rs372497074 | in-del | -/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997828 | TACTGAGGCACCCAC[-/T]TTTTTTTTTTTTTTT | 79058 |
rs372515682 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81979701 | CTGTAGGTTTTATTG[C/T]ATTGAGTTGCATAAG | 79058 |
rs372544716 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016601 | GAGCCAGCTGCCCGG[A/G]AGGGCGTTCGGTCTG | 79058 |
rs372553777 | in-del | -/G | 0.0494327 | 0.149241 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981346 | CTGGTTCAGTTGGTT[-/G]GGGGGGGCTTAGGGT | 79058 |
rs372687952 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001912 | CTGCCACACCGTAAC[A/G]TGCCCAGCTCCAGAC | 79058 |
rs372697330 | snp | C/G/T | 6.45946e-05 | 0.0056827 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996045 | GTCGCTGGGCCTGAC[C/G/T]GGGGGCAGCGCCACC | 79058 |
rs372730667 | snp | C/T | 0.000151451 | 0.00870073 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996020 | CTGCCCTGCGGGGCA[C/T]GACGCTGCAGTCGCT | 79058 |
rs372738512 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003853 | GCCTCCGAGGGTGGC[C/T]GGGGCGCTGAGTAAC | 79058 |
rs372744715 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984810 | CCACACACCCACATA[C/T]CCGCACACCCGTACA | 79058 |
rs372787473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001645 | GGGAGTGTGGGGCTC[C/T]GTACTGGGCGAGTCG | 79058 |
rs372787842 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009631 | CCCCCGTGAGGTCTG[C/T]GGACGGGATGGGGCG | 79058 |
rs372804527 | snp | C/G | 0.000437904 | 0.0147905 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016584 | CCTGTCCCTGGACCT[C/G]AGAGCCAGCTGCCCG | 79058 |
rs372844147 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997143 | GCTCCGGGATGAGGC[C/T]GTGTTGGCTCCATGA | 79058 |
rs372862837 | snp | A/G | 6.63042e-05 | 0.0057574 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81985531 | GCTTTGCAGCTGGAC[A/G]ATGGCTCGAGGTTGC | 79058 |
rs372882580 | snp | A/T | | | upstream-variant-2KB, intron-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977294 | AGCAGGGCACCGAGC[A/T]GGGGACGTGTCAGGG | 79058 |
rs373021309 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991717 | CGGCTGGGCTGTCAT[A/G]TGGTGGGTGATGCCC | 79058 |
rs373075414 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003949 | CACACTCCCTCTCAC[C/T]GGAGCCCTGGCGGGG | 79058 |
rs373238486 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005915 | GGGTGTGTGAGAGCC[A/G]CCTCCCCCATGCGGT | 79058 |
rs373257145 | in-del | -/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009791 | TCTGAGGGGGCCCCC[-/T]GTGAGGTCTGTGGAT | 79058 |
rs373257773 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005628 | TTGGGCCTCATTCCC[C/T]GCTGGCCCTCCGTCT | 79058 |
rs373269498 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981313 | AAGGTTTCTGGGGTC[C/T]CCTGGGCCAAGAGGA | 79058 |
rs373301255 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994741 | CACACCTTTGCTTTC[C/T]GAGTCTCCTGCCCCA | 79058 |
rs373309597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003434 | GCCTGGGCAACAGAG[C/T]GAGACGCTGTCTCAA | 79058 |
rs373362351 | snp | G/T | 1.66902e-05 | 0.00288874 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994775 | CCTCCGTGGCACTGG[G/T]TGAGCTGCCCTGGGG | 79058 |
rs373411465 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013876 | GGGCTGGCCCTGCCC[G/T]GGTGTCCTCACACAG | 79058 |
rs373433022 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995394 | GAGGTTCAGGTCTAC[A/G]TCCTCCCTTGAGGGG | 79058 |
rs373453499 | snp | A/G | 5.05046e-05 | 0.00502491 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011501 | CAGCCCGGGGCTGGC[A/G]TGGTGGAAGAGCTGT | 79058 |
rs373457707 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995600 | CGATCCCTGCCCACC[C/T]CGAGCTGAGCACCAG | 79058 |
rs373475808 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990678 | ATAGGAGACGCATGA[A/G]ATGGAAATGAGGATT | 79058 |
rs373485471 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015935 | TGTCCCTGGGCCCCC[A/G]GCTGGAGGCTGAGGT | 79058 |
rs373488327 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982811 | TCTTTTCTTTTCTTT[C/T]CTTTCCTTTCCTTTT | 79058 |
rs373541058 | snp | C/T | 8.22064e-05 | 0.00641065 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015035 | CTTCCCGGGCCCTGC[C/T]CTGGCTGGGGGGACG | 79058 |
rs373595080 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009635 | CAGTCGCCCCATCCC[A/G]TCCACAGACCTCACG | 79058 |
rs373635581 | snp | C/T | 1.66065e-05 | 0.00288149 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82011571 | AGACTTCGTGAGGAG[C/T]CACCTGGGGAACCCC | 79058 |
rs373654070 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984760 | AGTTCACTCCTGTGG[C/T]GCCTGCATGTACCCA | 79058 |
rs373664692 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000368 | GGAGCGTGTGCCTGG[C/T]CTGCATGGCGTGCTG | 79058 |
rs373744593 | snp | C/T | 8.34523e-05 | 0.00645904 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82010853 | CTACAGGGCTTCTTC[C/T]GCCCCAGCGAGACAG | 79058 |
rs373747797 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009703 | GACAGGACGTGGTGG[C/T]GACTGAGGCACAGCT | 79058 |
rs373812733 | snp | C/T | 0.000431616 | 0.0146841 | synonymous-codon, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015308 | TCGTCCGAGCAGTGG[C/T]GATCCCTCCCGAGTC | 79058 |
rs373826410 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004164 | GTGCATGCCCCTGGC[A/G]CCCTCACCCTGCAGC | 79058 |
rs373834783 | snp | C/T | 0.000117158 | 0.00765279 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016893 | CGGTGGGTCTGGGGG[C/T]ACCTCCCGTGGCGGC | 79058 |
rs373848028 | snp | C/T | 1.73177e-05 | 0.00294254 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996479 | GCCTGGGCTCGTCAG[C/T]GTCGGCTGGCCAGGC | 79058 |
rs373865623 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978832 | GTGCCAGAGCCAGGG[A/G]GTAGCTTGTGCTAGG | 79058 |
rs373895104 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983927 | CAGTGGCGCAGTCTC[A/G]GCTCACTTCAAGCTC | 79058 |
rs373915616 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982377 | CCATAGCCATGTTTT[C/G]AGGTGCCCTTTTCCT | 79058 |
rs373929219 | snp | C/T | 1.92814e-05 | 0.00310489 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81983572 | TCAGAGGAGCGTGCT[C/T]GACCTTTCTCTCCAG | 79058 |
rs373943690 | snp | C/T | 0.000465968 | 0.0152567 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011617 | CTGTGTACGTTTTTT[C/T]TCCTGAGCCCACTCC | 79058 |
rs373963664 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81980107 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGAGATTA | 79058 |
rs373986678 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000213 | TCAGCCCCTTCCCTC[C/T]GTGACCAGGGCGGGT | 79058 |
rs373997068 | snp | C/G | 6.20521e-05 | 0.00556976 | missense, nc-transcript-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009528 | GACCAAGGCCTTCAG[C/G]GAGGCGCAGATAAAG | 79058 |
rs374009388 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008582 | AGAGGGAGGGGCCGG[A/C]TTGTTCCCTGGGGGC | 79058 |
rs374059837 | in-del | -/GATC | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986577 | CTGTCCACAGTAAAA[-/GATC]GGCTCAGCAGAATGG | 79058 |
rs374074151 | snp | A/C/G | 5.03574e-05 | 0.00501763 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82017273 | GGGTGGTGAGAGCCC[A/C/G]GGGTGTGTGGTCACC | 79058 |
rs374173492 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983509 | TGGATGGCAGGGCGT[A/G]TCAGGCTCTGCAGGG | 79058 |
rs374191743 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82016865 | GCCGATGTGCTGGTG[A/G]CCAGGTAAGTGCCGG | 79058 |
rs374234352 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011978 | TCTAGGTGGCAAAGG[A/G]TTAGGCTGCCCACTG | 79058 |
rs374259051 | in-del | -/AGGGTGGGTCTGTGCATGCTGC | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991497 | CCTGTGGCCACACTC[-/AGGGTGGGTCTGTGCATGCTGC]TGGGCCAGCTCAGAG | 79058 |
rs374282396 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010743 | GAGTGGGGAGGCCAC[A/G]CCCTGGTCCCTGGTG | 79058 |
rs374291503 | in-del | -/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81979983 | TCTGGTGTTTTTTTT[-/T]GTTTTGTTTTGTTTT | 79058 |
rs374393413 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993331 | CCATTCTCCTGCCTC[A/G]GCCTCCCGAGTAGCT | 79058 |
rs374410137 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007399 | ACAGCCCCCTAGCAG[C/T]GTGATGCTGATGGTC | 79058 |
rs374443391 | snp | C/T | 6.47801e-05 | 0.00569086 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996023 | CCCTGCGGGGCACGA[C/T]GCTGCAGTCGCTGGG | 79058 |
rs374499838 | snp | A/G | 1.68855e-05 | 0.00290559 | utr-variant-3-prime, nc-transcript-variant, missense | ASPSCR1 | GRCh38.p7 | 17:82017339 | AGCTGCCAGCCTGAG[A/G]TGCCCACTCCGCCAG | 79058 |
rs374521150 | snp | C/T | 0.000117173 | 0.0076533 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81994860 | GGCCACCCCAGTCTG[C/T]GTGTACACGAGGGAT | 79058 |
rs374526963 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007497 | TGTCCAGTATGCGGA[C/T]GTGGCAGCAGCCCAC | 79058 |
rs374727465 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012456 | TCTGAAGTTGCTTCT[A/G]ACACGGCTTTCCGGC | 79058 |
rs374734789 | snp | G/T | 1.6582e-05 | 0.00287936 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81985518 | CCAGGTTCGCATCGC[G/T]TTGCAGCTGGACGAT | 79058 |
rs374754411 | in-del | -/A | 0.00292112 | 0.0381055 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81996105 | GGAGTCTATTTAGCT[-/A]AAAAAAAAAAGTGGT | 79058 |
rs374755001 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006326 | GTCCTTGCGGGTGCA[C/T]GTGTGCTTGGGTGCA | 79058 |
rs374772892 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992602 | ATCTGTGTCATGCTG[A/G]GGAGCGGGGACCCTG | 79058 |
rs374792021 | snp | C/T | 0.00125 | 0.0249687 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009024 | CGCCGTCAGCCGCGC[C/T]CTCTGCCTCCAGCCC | 79058 |
rs374873070 | snp | A/G | 8.94414e-05 | 0.00668676 | missense, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015226 | GTCCATCCAGAGGCC[A/G]AGCCTCTCCAAGCAC | 79058 |
rs374900977 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005462 | TTCTGGAAGGCTCCT[C/T]CTGGCTCTCAGCCAC | 79058 |
rs374927919 | snp | C/T | 0.000133043 | 0.00815498 | intron-variant, missense | ASPSCR1 | GRCh38.p7 | 17:82012209 | CGGTGCTTCCTAACA[C/T]GTAGGTGCCTTCTCT | 79058 |
rs374950484 | snp | C/T | | | intron-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009582 | GGTCTGCAGACAGGA[C/T]GTGGGGGCGACTGAG | 79058 |
rs374988082 | snp | A/G | 0.000198393 | 0.00995777 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016544 | TGAGTGTCAGTGGTT[A/G]GGGCCAGTGTCGGAG | 79058 |
rs374992477 | snp | C/T | 3.33072e-05 | 0.00408075 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011621 | GTACGTTTTTTCTCC[C/T]GAGCCCACTCCTGCC | 79058 |
rs375037364 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000419 | TGGGCAGCTGATTGA[C/T]GGAGGGCGTCCTGCC | 79058 |
rs375085352 | in-del | CGTA/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009640 | GGTCTGTGGACGGGA[CGTA/T]GGGGCGACTGAGGCA | 79058 |
rs375144552 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82017250 | GCCGGGCTGGTGGGC[A/G]GGTGGCCGGGTGGTG | 79058 |
rs375158730 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985138 | AACATGCACACACAC[A/G]CACATCTGCACGCAC | 79058 |
rs375238125 | snp | C/T | 0.000199041 | 0.00997402 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81985512 | TACCCTCCAGGTTCG[C/T]ATCGCTTTGCAGCTG | 79058 |
rs375266185 | in-del | A/TTT | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010102 | GTTTTTTTTTTTTTT[A/TTT]CTAGAGATGGAGTTT | 79058 |
rs375315509 | snp | C/T | 7.04411e-05 | 0.00593427 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994910 | TGCTCACCCAGTCCC[C/T]GCTCACTTTCAGCCC | 79058 |
rs375321478 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991432 | TGGGTGTGCTGGGGT[A/G]TAGGGATGGGCTGCT | 79058 |
rs375330067 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990703 | AGGATTTCATGGCCT[A/G]CGGGCCCTGGGGGTA | 79058 |
rs375365227 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010742 | CGAGTGGGGAGGCCA[C/T]GCCCTGGTCCCTGGT | 79058 |
rs375380328 | snp | A/G | | | downstream-variant-500B, intron-variant, synonymous-codon | ASPSCR1 | GRCh38.p7 | 17:82017431 | GTCATGCTTCCTCCA[A/G]AAAAGGGCCCCCGTC | 79058 |
rs375399436 | snp | C/T | 0.000305691 | 0.0123593 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983713 | TGTGGGGCACAGGAT[C/T]GTTCAGCTGGCCAGG | 79058 |
rs375409228 | snp | C/G | | | upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977435 | CCAAGCCGCGCTTCC[C/G]GGAGGCAGAGGACGA | 79058 |
rs375427472 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011209 | GCTGTGACATTCAGG[A/G]GCTTGTGACCTGTAC | 79058 |
rs375476528 | snp | G/T | 1.83886e-05 | 0.00303216 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81983636 | CTGGAGATGGTGCCC[G/T]CTTCCCGGAGCCGTG | 79058 |
rs375486854 | snp | A/G | 1.69115e-05 | 0.00290782 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996754 | CCTGGAGGCCCCTCC[A/G]AGCCAAAGAAGTCCA | 79058 |
rs375508428 | snp | A/C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005391 | GCGCCTGTGTGCCCC[A/C/G]TGGGTCGGCAGGTCT | 79058 |
rs375509452 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989670 | GTGATTTCCTTGGAT[A/G]GACACTGCCACGTGT | 79058 |
rs375518305 | snp | A/G | 7.15871e-05 | 0.00598234 | missense, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015271 | GCCACCCAGTCTGCC[A/G]ACCCTCCTCTCCACC | 79058 |
rs375560510 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982582 | TGGCCAGTGTTGATA[C/T]AGCAAAGTTTGTTCT | 79058 |
rs375570693 | snp | A/G | 3.29533e-05 | 0.00405901 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81979203 | TGGAGGACACGTGCC[A/G]GCGGCAGGACTTCAA | 79058 |
rs375727115 | snp | A/G/T | 8.62499e-05 | 0.00656646 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996554 | GCGGCGACTTGAGCC[A/G/T]TCCGGAGGACGCGGA | 79058 |
rs375823500 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002497 | TGACCTCAGGTGATC[C/T]ACTTGCATCGGCCTC | 79058 |
rs375859557 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990494 | GCCTGTGTCTGAGTT[C/T]GGGATCTTCCACGCC | 79058 |
rs375918514 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81979609 | CTTCAAAGACCAGGA[C/T]CCCTAGTAAGATGTT | 79058 |
rs375929531 | snp | A/T | 2.15028e-05 | 0.00327886 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996022 | GCCCTGCGGGGCACG[A/T]CGCTGCAGTCGCTGG | 79058 |
rs375953318 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004379 | TGGTTAGCATCATTG[C/T]GGTCCGGTCCTTGGC | 79058 |
rs375959579 | in-del | -/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007318 | CCCTTGGGATGACGG[-/G]TAGGAATCTAGGGTG | 79058 |
rs375972930 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989297 | GGAGCAGGATATGGA[C/T]GAGGTTTCATAGTGG | 79058 |
rs376082275 | snp | A/G | 7.85207e-05 | 0.00626531 | intron-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009591 | ACAGGATGTGGGGGC[A/G]ACTGAGGCACAGCTC | 79058 |
rs376097160 | snp | C/G | 0.000149636 | 0.00864843 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983527 | AGGCTCTGCAGGGCA[C/G]CAAGTGTGCTCTGGT | 79058 |
rs376104812 | snp | C/T | 9.01299e-05 | 0.00671244 | missense, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015126 | GGTCCCTCGCTGAAA[C/T]GGTGCCTGGGACCAG | 79058 |
rs376118592 | snp | G/T | 0.00199481 | 0.0315187 | downstream-variant-500B, intron-variant, missense | ASPSCR1 | GRCh38.p7 | 17:82017539 | TGGTGGACCGTGGTG[G/T]GCATCCTGAACCCGC | 79058 |
rs376138915 | snp | A/G | 0.000434986 | 0.0147412 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985612 | CCACAGATCAGGTGA[A/G]CATCAGTGGGCTGGG | 79058 |
rs376202673 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981882 | TGTGGACCAGGCTGG[C/T]CTCAAACTCCTGACC | 79058 |
rs376254775 | snp | C/T | 3.6916e-05 | 0.00429612 | synonymous-codon, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015341 | GGCTGGGCACAAGCA[C/T]GTGGGGACAGGCCGG | 79058 |
rs376333757 | snp | C/T | 8.36225e-05 | 0.00646562 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016878 | TGGCCAGGTAAGTGC[C/T]GGTGGGTCTGGGGGC | 79058 |
rs376379847 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987497 | CACAGGCACAGGTGC[G/T]TGGTGAGGGCCGTCC | 79058 |
rs376429819 | in-del | -/T | 0 | 0 | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81975781 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTTGC | 79058 |
rs376449502 | in-del | -/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991483 | GGTGGAGCACTGGCC[-/T]TGTGGCCACACTCAG | 79058 |
rs376475909 | in-del | -/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983862 | AATGAGCATCTCATG[-/T]TTTTTTTTTTTTTGA | 79058 |
rs376496415 | snp | C/T | 0.000437904 | 0.0147905 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81979115 | CTGAATGCCCTTGGC[C/T]GACCTGGCCCACTGC | 79058 |
rs376519963 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994753 | TTCCGAGTCTCCTGC[C/G]CCAGGGCCTCCGTGG | 79058 |
rs376526605 | snp | A/C/G | 0.000174115 | 0.00932904 | utr-variant-3-prime, nc-transcript-variant, synonymous-codon | ASPSCR1 | GRCh38.p7 | 17:82017341 | CTGCCAGCCTGAGGT[A/C/G]CCCACTCCGCCAGCC | 79058 |
rs376604718 | snp | G/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003964 | CGGAGCCCTGGCGGG[G/T]CAGGCCGGGCCGAGA | 79058 |
rs376636450 | snp | A/G | 1.88496e-05 | 0.00306993 | intron-variant, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996879 | CCTTGGGACTTGGGG[A/G]TGTCCTTTCTCCTGA | 79058 |
rs376642185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81979611 | TCAAAGACCAGGATC[C/T]CTAGTAAGATGTTCA | 79058 |
rs376642308 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81998798 | CTTTTCTGGGTTCTG[C/G]AAGTTCTCCGAAGGT | 79058 |
rs376733139 | snp | A/G | 4.30098e-05 | 0.00463714 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996050 | TGGGCCTGACCGGGG[A/G]CAGCGCCACCATCAG | 79058 |
rs376741546 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991480 | GCCAGGTGGAGCACT[C/G]GCCTGTGGCCACACT | 79058 |
rs376789001 | snp | C/G/T | 0.000399265 | 0.0141237 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985493 | GGAAGTTTCTCATGT[C/G/T]TTATACCCTCCAGGT | 79058 |
rs376790773 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81996254 | ACCTCATCTCTGTGT[C/T]CCCCAGAGGGGCGGT | 79058 |
rs376855821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992830 | CGGGAGCTTAGGGAG[C/T]GTGTCCCAGCCTGTG | 79058 |
rs376911078 | snp | A/G | 0.000179984 | 0.0094847 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009010 | CAGCCCGTGACACCC[A/G]CCGTCAGCCGCGCCC | 79058 |
rs377043670 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004626 | ATGTGGCAGCCACAG[A/G/T]CACCCCCACCCTGTG | 79058 |
rs377056314 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82017168 | TGGAGGGCGGGGGTC[C/T]GGGTGCTGTGGCAGG | 79058 |
rs377064037 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81998751 | GGAATCGAATTTCAC[C/G]TGGCTCACAAGGGAG | 79058 |
rs377065294 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81980065 | TTGGCTCACTGCAAC[C/T]TCCACCTCCTAGGTT | 79058 |
rs377074899 | snp | C/T | 0.000103912 | 0.00720731 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996498 | GGCTGGCCAGGCAGC[C/T]GCCAGCGCTCCACTT | 79058 |
rs377083417 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001715 | TGGACTCTCCTCCCC[A/G]TTGGGCCCAAGATCC | 79058 |
rs377216775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010443 | CTGAGGCAGGAGAAA[A/G]GCGTGAACCCGGGAG | 79058 |
rs377269518 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010600 | TAGAACGCAGGCCGC[C/T]GTGCACACACACGGC | 79058 |
rs377288926 | snp | C/G | 6.71163e-05 | 0.00579255 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82017316 | CACTACAGCCAGCAA[C/G]AGGTGAGAGCTGCCA | 79058 |
rs377309026 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983514 | GGCAGGGCGTGTCAG[C/G]CTCTGCAGGGCAGCA | 79058 |
rs377335608 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005802 | ACAGCCCCTGTCGGG[A/G]TGTGGGAAGGGGCGG | 79058 |
rs377336758 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991813 | GCATGCTGCTGCCTG[C/G]GCTCTCGTCAGCACC | 79058 |
rs377346402 | snp | A/T | 6.7005e-05 | 0.00578775 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011521 | GGAAGAGCTGTCTGT[A/T]TGTTCTTTTTCTCCT | 79058 |
rs377362663 | snp | G/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81996285 | GGATCTTGGGAGGGC[G/T]CATGGGGCAGGAGAG | 79058 |
rs377364189 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007816 | GCTGGGGCTGTGGGG[G/T]GCCGCCTGGCGCCTG | 79058 |
rs377390027 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014598 | GCCTCCCTCCCAGGC[A/G]CTGTGGTGCCGCCTC | 79058 |
rs377391034 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010662 | GGGGAGTCAAAGCCC[A/G]GGCCCTGATTGGGGG | 79058 |
rs377398059 | snp | C/T | 0.000422494 | 0.0145282 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82016986 | CCCATTGCCAGCCCC[C/T]GACCCTGCACCTAAG | 79058 |
rs377403408 | snp | A/G | 0.000169808 | 0.00921278 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994885 | AGGGATGAGGTAGGC[A/G]GCCTGCTCTTGCTCA | 79058 |